Linked Data
ClinVar Variation Id:
183134
ClinVar RCV Id:
RCV000162014
dbSNP Id:
rs730882114
ExAC:
19:11238728 A / G
gnomAD v2:
19-11238728-A-G
gnomAD v4:
19-11128052-A-G
PubMed:
PMID:25647241
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11128052A>G , CM000681.2:g.11128052A>G | GRCh38 |
| NC_000019.9:g.11238728A>G , CM000681.1:g.11238728A>G | GRCh37 |
| NC_000019.8:g.11099728A>G | NCBI36 |
| NG_009060.1:g.43672A>G , LRG_274:g.43672A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2614A>G | ENSP00000252444.6:p.Ser872Gly | |
| ENST00000559340.2:c.*425A>G | ENSP00000453696.2:n.*425A>G | |
| ENST00000560467.2:c.2236A>G | ENSP00000453513.2:p.Ser746Gly | |
| ENST00000558518.6:c.2356A>G MANE Select | ENSP00000454071.1:p.Ser786Gly | |
| ENST00000252444.9:c.2610A>G | ||
| ENST00000455727.6:c.1852A>G | ENSP00000397829.2:p.Ser618Gly | |
| ENST00000535915.5:c.2233A>G | ENSP00000440520.1:p.Ser745Gly | |
| ENST00000545707.5:c.1822A>G | ENSP00000437639.1:p.Ser608Gly | |
| ENST00000557933.5:c.2356A>G | ENSP00000453557.1:p.Ser786Gly | |
| ENST00000558013.5:c.2356A>G | ENSP00000453346.1:p.Ser786Gly | |
| ENST00000558518.5:c.2356A>G | ENSP00000454071.1:p.Ser786Gly | |
| ENST00000560628.1:n.108+398A>G | ||
| NM_000527.4:c.2356A>G , LRG_274t1:c.2356A>G | NP_000518.1:p.Ser786Gly | |
| NM_001195798.1:c.2356A>G | NP_001182727.1:p.Ser786Gly | |
| NM_001195799.1:c.2233A>G | NP_001182728.1:p.Ser745Gly | |
| NM_001195800.1:c.1852A>G | NP_001182729.1:p.Ser618Gly | |
| NM_001195803.1:c.1822A>G | NP_001182732.1:p.Ser608Gly | |
| XM_011528010.1:c.2312-1461A>G | XP_011526312.1:n.2312-1461A>G | |
| XM_011528011.1:c.1975A>G | XP_011526313.1:p.Ser659Gly | |
| XR_244074.2:n.2366A>G | ||
| XM_011528010.2:c.2312-1461A>G | XP_011526312.1:n.2312-1461A>G | |
| XR_001753685.2:n.2690A>G | ||
| XR_001753686.2:n.2333A>G | ||
| NM_000527.5:c.2356A>G MANE Select | NP_000518.1:p.Ser786Gly | |
| NM_001195798.2:c.2356A>G | NP_001182727.1:p.Ser786Gly | |
| NM_001195799.2:c.2233A>G | NP_001182728.1:p.Ser745Gly | |
| NM_001195800.2:c.1852A>G | NP_001182729.1:p.Ser618Gly | |
| NM_001195803.2:c.1822A>G | NP_001182732.1:p.Ser608Gly |