Linked Data
ClinVar Variation Id:
252184
ClinVar RCV Id:
RCV000237441
dbSNP Id:
rs879255118
PubMed:
PMID:9409298
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11120423T>A , CM000681.2:g.11120423T>A | GRCh38 |
| NC_000019.9:g.11231099T>A , CM000681.1:g.11231099T>A | GRCh37 |
| NC_000019.8:g.11092099T>A | NCBI36 |
| NG_009060.1:g.36043T>A , LRG_274:g.36043T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2299T>A | ENSP00000252444.6:p.Cys767Ser | |
| ENST00000559340.2:c.*110T>A | ENSP00000453696.2:n.*110T>A | |
| ENST00000560467.2:c.1921T>A | ENSP00000453513.2:p.Cys641Ser | |
| ENST00000558518.6:c.2041T>A MANE Select | ENSP00000454071.1:p.Cys681Ser | |
| ENST00000252444.9:c.2295T>A | ||
| ENST00000455727.6:c.1537T>A | ENSP00000397829.2:p.Cys513Ser | |
| ENST00000535915.5:c.1918T>A | ENSP00000440520.1:p.Cys640Ser | |
| ENST00000545707.5:c.1606+190T>A | ENSP00000437639.1:n.1606+190T>A | |
| ENST00000557933.5:c.2041T>A | ENSP00000453557.1:p.Cys681Ser | |
| ENST00000558013.5:c.2041T>A | ENSP00000453346.1:p.Cys681Ser | |
| ENST00000558518.5:c.2041T>A | ENSP00000454071.1:p.Cys681Ser | |
| NM_000527.4:c.2041T>A , LRG_274t1:c.2041T>A | NP_000518.1:p.Cys681Ser | |
| NM_001195798.1:c.2041T>A | NP_001182727.1:p.Cys681Ser | |
| NM_001195799.1:c.1918T>A | NP_001182728.1:p.Cys640Ser | |
| NM_001195800.1:c.1537T>A | NP_001182729.1:p.Cys513Ser | |
| NM_001195803.1:c.1606+190T>A | NP_001182732.1:n.1606+190T>A | |
| XM_011528010.1:c.2041T>A | XP_011526312.1:p.Cys681Ser | |
| XM_011528011.1:c.1660T>A | XP_011526313.1:p.Cys554Ser | |
| XR_244074.2:n.2051T>A | ||
| XM_011528010.2:c.2041T>A | XP_011526312.1:p.Cys681Ser | |
| XR_001753685.2:n.2158T>A | ||
| XR_001753686.2:n.2018T>A | ||
| NM_000527.5:c.2041T>A MANE Select | NP_000518.1:p.Cys681Ser | |
| NM_001195798.2:c.2041T>A | NP_001182727.1:p.Cys681Ser | |
| NM_001195799.2:c.1918T>A | NP_001182728.1:p.Cys640Ser | |
| NM_001195800.2:c.1537T>A | NP_001182729.1:p.Cys513Ser | |
| NM_001195803.2:c.1606+190T>A | NP_001182732.1:n.1606+190T>A |