Linked Data
ClinVar Variation Id:
574403
dbSNP Id:
rs186508321
gnomAD v2:
18-52921795-C-A
gnomAD v3:
18-55254564-C-A
gnomAD v4:
18-55254564-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.55254564C>A , CM000680.2:g.55254564C>A | GRCh38 |
| NC_000018.9:g.52921795C>A , CM000680.1:g.52921795C>A | GRCh37 |
| NC_000018.8:g.51072793C>A | NCBI36 |
| NG_011716.1:g.339066G>T | |
| NG_011716.2:g.386430G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354452.8:c.1283G>T MANE Select | ENSP00000346440.3:p.Gly428Val | |
| ENST00000630720.3:c.800G>T | ENSP00000487218.1:p.Gly267Val | |
| ENST00000635822.2:c.1283G>T | ENSP00000490451.1:p.Gly428Val | |
| ENST00000635990.2:n.963G>T | ||
| ENST00000636400.2:c.1211G>T | ENSP00000490006.1:p.Gly404Val | |
| ENST00000636751.2:c.*991G>T | ENSP00000489783.1:n.*991G>T | |
| ENST00000636822.2:c.893G>T | ENSP00000490883.1:p.Gly298Val | |
| ENST00000637115.2:c.*1173G>T | ENSP00000490234.1:n.*1173G>T | |
| ENST00000637169.2:c.635G>T | ENSP00000490832.1:p.Gly212Val | |
| ENST00000637239.2:n.1350G>T | ||
| ENST00000637250.2:n.977G>T | ||
| ENST00000637923.2:c.881G>T | ||
| ENST00000638154.3:c.1310G>T | ENSP00000490625.2:p.Gly437Val | |
| ENST00000643689.1:c.893G>T | ENSP00000494380.1:p.Gly298Val | |
| ENST00000674764.1:c.*894G>T | ENSP00000502213.1:n.*894G>T | |
| ENST00000675707.1:c.893G>T | ENSP00000501758.1:p.Gly298Val | |
| ENST00000354452.7:c.1283G>T | ENSP00000346440.3:p.Gly428Val | |
| ENST00000356073.8:c.1283G>T | ENSP00000348374.4:p.Gly428Val | |
| ENST00000398339.5:c.1589G>T | ENSP00000381382.1:p.Gly530Val | |
| ENST00000457482.7:c.803G>T | ENSP00000409447.2:p.Gly268Val | |
| ENST00000537578.5:c.1211G>T | ENSP00000440731.1:p.Gly404Val | |
| ENST00000537856.7:c.893G>T | ENSP00000439827.2:p.Gly298Val | |
| ENST00000540999.5:c.1211G>T | ENSP00000445202.1:p.Gly404Val | |
| ENST00000543082.5:c.1157G>T | ENSP00000439656.1:p.Gly386Val | |
| ENST00000544241.6:c.1070G>T | ENSP00000441562.2:p.Gly357Val | |
| ENST00000561831.7:c.803G>T | ENSP00000457765.1:p.Gly268Val | |
| ENST00000561992.5:c.893G>T | ENSP00000455179.1:p.Gly298Val | |
| ENST00000562680.5:n.1374G>T | ||
| ENST00000563760.5:n.796G>T | ||
| ENST00000564228.5:c.1070G>T | ENSP00000455261.1:p.Gly357Val | |
| ENST00000564403.6:c.1301G>T | ENSP00000457263.1:p.Gly434Val | |
| ENST00000564999.5:c.1283G>T | ENSP00000457649.1:p.Gly428Val | |
| ENST00000565018.6:c.1031G>T | ENSP00000455984.2:p.Gly344Val | |
| ENST00000566279.5:c.1103G>T | ENSP00000456125.1:p.Gly368Val | |
| ENST00000566286.5:c.1274G>T | ENSP00000455418.2:p.Gly425Val | |
| ENST00000567880.5:c.1103G>T | ENSP00000454366.1:p.Gly368Val | |
| ENST00000568673.5:c.1211G>T | ENSP00000455135.1:p.Gly404Val | |
| ENST00000568740.5:c.1208G>T | ENSP00000455346.1:p.Gly403Val | |
| ENST00000570177.6:c.893G>T | ENSP00000454647.1:p.Gly298Val | |
| ENST00000570287.6:c.803G>T | ENSP00000455763.1:p.Gly268Val | |
| ENST00000616053.4:c.1031G>T | ENSP00000478549.1:p.Gly344Val | |
| ENST00000626466.1:n.318G>T | ||
| ENST00000626584.2:c.635G>T | ENSP00000486072.1:p.Gly212Val | |
| ENST00000629387.2:c.1283G>T | ENSP00000486670.1:p.Gly428Val | |
| ENST00000630720.2:c.800G>T | ENSP00000487218.1:p.Gly267Val | |
| NM_001083962.1:c.1283G>T | NP_001077431.1:p.Gly428Val | |
| NM_001243226.2:c.1589G>T | NP_001230155.2:p.Gly530Val | |
| NM_001243227.1:c.1211G>T | NP_001230156.1:p.Gly404Val | |
| NM_001243228.1:c.1301G>T | NP_001230157.1:p.Gly434Val | |
| NM_001243230.1:c.1274G>T | NP_001230159.1:p.Gly425Val | |
| NM_001243231.1:c.1157G>T | NP_001230160.1:p.Gly386Val | |
| NM_001243232.1:c.1070G>T | NP_001230161.1:p.Gly357Val | |
| NM_001243233.1:c.893G>T | NP_001230162.1:p.Gly298Val | |
| NM_001243234.1:c.803G>T | NP_001230163.1:p.Gly268Val | |
| NM_001243235.1:c.803G>T | NP_001230164.1:p.Gly268Val | |
| NM_001243236.1:c.803G>T | NP_001230165.1:p.Gly268Val | |
| NM_001306207.1:c.1211G>T | NP_001293136.1:p.Gly404Val | |
| NM_001306208.1:c.1070G>T | NP_001293137.1:p.Gly357Val | |
| NM_003199.2:c.1283G>T | NP_003190.1:p.Gly428Val | |
| XM_005266739.3:c.1211G>T | XP_005266796.2:p.Gly404Val | |
| XM_005266741.3:c.1280G>T | XP_005266798.1:p.Gly427Val | |
| XM_005266743.3:c.1211G>T | XP_005266800.1:p.Gly404Val | |
| XM_005266744.3:c.1211G>T | XP_005266801.1:p.Gly404Val | |
| XM_005266745.3:c.1208G>T | XP_005266802.1:p.Gly403Val | |
| XM_005266747.3:c.1157G>T | XP_005266804.1:p.Gly386Val | |
| XM_005266749.3:c.1073G>T | XP_005266806.1:p.Gly358Val | |
| XM_005266752.3:c.893G>T | XP_005266809.1:p.Gly298Val | |
| XM_005266754.3:c.893G>T | XP_005266811.1:p.Gly298Val | |
| XM_005266755.3:c.893G>T | XP_005266812.1:p.Gly298Val | |
| XM_005266761.3:c.800G>T | XP_005266818.1:p.Gly267Val | |
| XM_006722536.2:c.1283G>T | XP_006722599.1:p.Gly428Val | |
| XM_006722537.2:c.1283G>T | XP_006722600.1:p.Gly428Val | |
| XM_006722538.2:c.1208G>T | XP_006722601.1:p.Gly403Val | |
| XM_006722539.2:c.893G>T | XP_006722602.1:p.Gly298Val | |
| XM_006722540.2:c.893G>T | XP_006722603.1:p.Gly298Val | |
| XM_011526154.1:c.1586G>T | XP_011524456.1:p.Gly529Val | |
| XM_011526155.1:c.1586G>T | XP_011524457.1:p.Gly529Val | |
| XM_011526156.1:c.1589G>T | XP_011524458.1:p.Gly530Val | |
| XM_011526157.1:c.1586G>T | XP_011524459.1:p.Gly529Val | |
| XM_011526158.1:c.1277G>T | XP_011524460.1:p.Gly426Val | |
| XM_011526159.1:c.893G>T | XP_011524461.1:p.Gly298Val | |
| XM_011526160.1:c.893G>T | XP_011524462.1:p.Gly298Val | |
| XM_011526161.1:c.893G>T | XP_011524463.1:p.Gly298Val | |
| XM_011526162.1:c.893G>T | XP_011524464.1:p.Gly298Val | |
| XM_011526163.1:c.893G>T | XP_011524465.1:p.Gly298Val | |
| XM_011526164.1:c.893G>T | XP_011524466.1:p.Gly298Val | |
| NM_001330604.2:c.1280G>T | NP_001317533.1:p.Gly427Val | |
| NM_001330605.2:c.893G>T | NP_001317534.1:p.Gly298Val | |
| NM_001348211.1:c.1157G>T | NP_001335140.1:p.Gly386Val | |
| NM_001348212.1:c.893G>T | NP_001335141.1:p.Gly298Val | |
| NM_001348213.1:c.893G>T | NP_001335142.1:p.Gly298Val | |
| NM_001348214.1:c.800G>T | NP_001335143.1:p.Gly267Val | |
| NM_001348215.1:c.635G>T | NP_001335144.1:p.Gly212Val | |
| NM_001348216.1:c.803G>T | NP_001335145.1:p.Gly268Val | |
| NM_001348217.1:c.1211G>T | NP_001335146.1:p.Gly404Val | |
| NM_001348218.1:c.1211G>T | NP_001335147.1:p.Gly404Val | |
| NM_001348219.1:c.1211G>T | NP_001335148.1:p.Gly404Val | |
| NM_001348220.1:c.1208G>T | NP_001335149.1:p.Gly403Val | |
| XM_005266739.4:c.1211G>T | XP_005266796.2:p.Gly404Val | |
| XM_005266741.4:c.1280G>T | XP_005266798.1:p.Gly427Val | |
| XM_005266745.4:c.1208G>T | XP_005266802.1:p.Gly403Val | |
| XM_005266749.4:c.1073G>T | XP_005266806.1:p.Gly358Val | |
| XM_005266752.5:c.893G>T | XP_005266809.1:p.Gly298Val | |
| XM_005266755.5:c.893G>T | XP_005266812.1:p.Gly298Val | |
| XM_005266761.4:c.800G>T | XP_005266818.1:p.Gly267Val | |
| XM_006722536.3:c.1283G>T | XP_006722599.1:p.Gly428Val | |
| XM_006722537.3:c.1283G>T | XP_006722600.1:p.Gly428Val | |
| XM_006722538.3:c.1208G>T | XP_006722601.1:p.Gly403Val | |
| XM_017025934.2:c.1208G>T | XP_016881423.1:p.Gly403Val | |
| XM_017025935.2:c.1208G>T | XP_016881424.1:p.Gly403Val | |
| XM_017025936.2:c.1211G>T | XP_016881425.1:p.Gly404Val | |
| XM_017025937.2:c.1208G>T | XP_016881426.1:p.Gly403Val | |
| XM_017025938.2:c.1280G>T | XP_016881427.1:p.Gly427Val | |
| XM_017025940.2:c.1283G>T | XP_016881429.1:p.Gly428Val | |
| XM_017025941.2:c.1283G>T | XP_016881430.1:p.Gly428Val | |
| XM_017025942.2:c.1280G>T | XP_016881431.1:p.Gly427Val | |
| XM_017025943.2:c.1280G>T | XP_016881432.1:p.Gly427Val | |
| XM_017025944.2:c.1208G>T | XP_016881433.1:p.Gly403Val | |
| XM_017025945.2:c.1208G>T | XP_016881434.1:p.Gly403Val | |
| XM_017025946.2:c.1211G>T | XP_016881435.1:p.Gly404Val | |
| XM_017025948.2:c.1208G>T | XP_016881437.1:p.Gly403Val | |
| XM_017025950.2:c.1205G>T | XP_016881439.1:p.Gly402Val | |
| XM_017025951.2:c.1154G>T | XP_016881440.1:p.Gly385Val | |
| XM_017025952.2:c.1067G>T | XP_016881441.1:p.Gly356Val | |
| XM_017025953.2:c.1073G>T | XP_016881442.1:p.Gly358Val | |
| XM_017025954.2:c.890G>T | XP_016881443.1:p.Gly297Val | |
| XM_017025956.2:c.893G>T | XP_016881445.1:p.Gly298Val | |
| XM_024451240.1:c.1208G>T | XP_024307008.1:p.Gly403Val | |
| XM_024451241.1:c.1046G>T | XP_024307009.1:p.Gly349Val | |
| NM_001083962.2:c.1283G>T MANE Select | NP_001077431.1:p.Gly428Val | |
| NM_001243226.3:c.1589G>T | NP_001230155.2:p.Gly530Val | |
| NM_001243227.2:c.1211G>T | NP_001230156.1:p.Gly404Val | |
| NM_001243228.2:c.1301G>T | NP_001230157.1:p.Gly434Val | |
| NM_001243231.2:c.1157G>T | NP_001230160.1:p.Gly386Val | |
| NM_001243233.2:c.893G>T | NP_001230162.1:p.Gly298Val | |
| NM_001243234.2:c.803G>T | NP_001230163.1:p.Gly268Val | |
| NM_001243235.2:c.803G>T | NP_001230164.1:p.Gly268Val | |
| NM_001243236.2:c.803G>T | NP_001230165.1:p.Gly268Val | |
| NM_001330604.3:c.1280G>T | NP_001317533.1:p.Gly427Val | |
| NM_001330605.3:c.893G>T | NP_001317534.1:p.Gly298Val | |
| NM_001348211.2:c.1157G>T | NP_001335140.1:p.Gly386Val | |
| NM_001348212.2:c.893G>T | NP_001335141.1:p.Gly298Val | |
| NM_001348213.2:c.893G>T | NP_001335142.1:p.Gly298Val | |
| NM_001348214.2:c.800G>T | NP_001335143.1:p.Gly267Val | |
| NM_001348215.2:c.635G>T | NP_001335144.1:p.Gly212Val | |
| NM_001348216.2:c.803G>T | NP_001335145.1:p.Gly268Val | |
| NM_001348218.2:c.1211G>T | NP_001335147.1:p.Gly404Val | |
| NM_001348219.2:c.1211G>T | NP_001335148.1:p.Gly404Val | |
| NM_001369567.1:c.1283G>T | NP_001356496.1:p.Gly428Val | |
| NM_001369568.1:c.1283G>T | NP_001356497.1:p.Gly428Val | |
| NM_001369569.1:c.1280G>T | NP_001356498.1:p.Gly427Val | |
| NM_001369570.1:c.1280G>T | NP_001356499.1:p.Gly427Val | |
| NM_001369571.1:c.1283G>T | NP_001356500.1:p.Gly428Val | |
| NM_001369572.1:c.1283G>T | NP_001356501.1:p.Gly428Val | |
| NM_001369573.1:c.1280G>T | NP_001356502.1:p.Gly427Val | |
| NM_001369574.1:c.1280G>T | NP_001356503.1:p.Gly427Val | |
| NM_001369575.1:c.1211G>T | NP_001356504.1:p.Gly404Val | |
| NM_001369576.1:c.1208G>T | NP_001356505.1:p.Gly403Val | |
| NM_001369577.1:c.1208G>T | NP_001356506.1:p.Gly403Val | |
| NM_001369578.1:c.1208G>T | NP_001356507.1:p.Gly403Val | |
| NM_001369579.1:c.1208G>T | NP_001356508.1:p.Gly403Val | |
| NM_001369580.1:c.1208G>T | NP_001356509.1:p.Gly403Val | |
| NM_001369581.1:c.1208G>T | NP_001356510.1:p.Gly403Val | |
| NM_001369582.1:c.1211G>T | NP_001356511.1:p.Gly404Val | |
| NM_001369583.1:c.1211G>T | NP_001356512.1:p.Gly404Val | |
| NM_001369584.1:c.1208G>T | NP_001356513.1:p.Gly403Val | |
| NM_001369585.1:c.1208G>T | NP_001356514.1:p.Gly403Val | |
| NM_001369586.1:c.1214G>T | NP_001356515.1:p.Gly405Val | |
| NM_003199.3:c.1283G>T | NP_003190.1:p.Gly428Val | |
| NM_001243230.2:c.1274G>T | NP_001230159.1:p.Gly425Val |