Linked Data
ClinVar Variation Id:
656182
dbSNP Id:
rs754115060
ExAC:
2:39250011 C / T
gnomAD v2:
2-39250011-C-T
gnomAD v3:
2-39022870-C-T
gnomAD v4:
2-39022870-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39022870C>T , CM000664.2:g.39022870C>T | GRCh38 |
| NC_000002.11:g.39250011C>T , CM000664.1:g.39250011C>T | GRCh37 |
| NC_000002.10:g.39103515C>T | NCBI36 |
| NG_007530.1:g.102594G>A , LRG_754:g.102594G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000472480.2:n.1438G>A | ||
| ENST00000685279.1:c.325G>A | ENSP00000509424.1:p.Asp109Asn | |
| ENST00000688043.1:n.1779G>A | ||
| ENST00000689668.1:n.1565G>A | ||
| ENST00000690876.1:c.1447G>A | ENSP00000508955.1:p.Asp483Asn | |
| ENST00000691229.1:c.1447G>A | ENSP00000510437.1:p.Asp483Asn | |
| ENST00000692089.1:c.1447G>A | ENSP00000508626.1:p.Asp483Asn | |
| ENST00000692620.1:c.325G>A | ENSP00000509311.1:p.Asp109Asn | |
| ENST00000402219.8:c.1558G>A MANE Select | ENSP00000384675.2:p.Asp520Asn | |
| ENST00000395038.6:c.1558G>A | ENSP00000378479.2:p.Asp520Asn | |
| ENST00000402219.6:c.1558G>A | ENSP00000384675.2:p.Asp520Asn | |
| ENST00000426016.5:c.1558G>A | ENSP00000387784.1:p.Asp520Asn | |
| NM_005633.3:c.1558G>A , LRG_754t1:c.1558G>A | NP_005624.2:p.Asp520Asn | |
| XM_005264515.3:c.1558G>A | XP_005264572.1:p.Asp520Asn | |
| XM_011533060.1:c.1651G>A | XP_011531362.1:p.Asp551Asn | |
| XM_011533061.1:c.1651G>A | XP_011531363.1:p.Asp551Asn | |
| XM_011533062.1:c.1537G>A | XP_011531364.1:p.Asp513Asn | |
| XM_011533063.1:c.1534G>A | XP_011531365.1:p.Asp512Asn | |
| XM_011533064.1:c.1387G>A | XP_011531366.1:p.Asp463Asn | |
| XM_011533065.1:c.1651G>A | XP_011531367.1:p.Asp551Asn | |
| XM_011533066.1:c.493G>A | XP_011531368.1:p.Asp165Asn | |
| XM_005264515.4:c.1558G>A | XP_005264572.1:p.Asp520Asn | |
| XM_011533062.2:c.1537G>A | XP_011531364.1:p.Asp513Asn | |
| XM_011533064.2:c.1387G>A | XP_011531366.1:p.Asp463Asn | |
| NM_001382394.1:c.1537G>A | NP_001369323.1:p.Asp513Asn | |
| NM_001382395.1:c.1558G>A | NP_001369324.1:p.Asp520Asn | |
| NM_005633.4:c.1558G>A MANE Select | NP_005624.2:p.Asp520Asn |