Linked Data
ClinVar Variation Id:
251540
dbSNP Id:
rs13306512
ExAC:
19:11218189 C / G
gnomAD v2:
19-11218189-C-G
gnomAD v3:
19-11107513-C-G
gnomAD v4:
19-11107513-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11107513C>G , CM000681.2:g.11107513C>G | GRCh38 |
| NC_000019.9:g.11218189C>G , CM000681.1:g.11218189C>G | GRCh37 |
| NC_000019.8:g.11079189C>G | NCBI36 |
| NG_009060.1:g.23133C>G , LRG_274:g.23133C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1197C>G | ENSP00000252444.6:p.Cys399Trp | |
| ENST00000559340.2:c.939C>G | ENSP00000453696.2:p.Cys313Trp | |
| ENST00000560467.2:c.939C>G | ENSP00000453513.2:p.Cys313Trp | |
| ENST00000558518.6:c.939C>G MANE Select | ENSP00000454071.1:p.Cys313Trp | |
| ENST00000252444.9:c.1193C>G | ||
| ENST00000455727.6:c.435C>G | ENSP00000397829.2:p.Cys145Trp | |
| ENST00000535915.5:c.816C>G | ENSP00000440520.1:p.Cys272Trp | |
| ENST00000545707.5:c.558C>G | ENSP00000437639.1:p.Cys186Trp | |
| ENST00000557933.5:c.939C>G | ENSP00000453557.1:p.Cys313Trp | |
| ENST00000558013.5:c.939C>G | ENSP00000453346.1:p.Cys313Trp | |
| ENST00000558518.5:c.939C>G | ENSP00000454071.1:p.Cys313Trp | |
| ENST00000558528.1:n.454C>G | ||
| ENST00000560467.1:c.539C>G | ||
| NM_000527.4:c.939C>G , LRG_274t1:c.939C>G | NP_000518.1:p.Cys313Trp | |
| NM_001195798.1:c.939C>G | NP_001182727.1:p.Cys313Trp | |
| NM_001195799.1:c.816C>G | NP_001182728.1:p.Cys272Trp | |
| NM_001195800.1:c.435C>G | NP_001182729.1:p.Cys145Trp | |
| NM_001195803.1:c.558C>G | NP_001182732.1:p.Cys186Trp | |
| XM_011528010.1:c.939C>G | XP_011526312.1:p.Cys313Trp | |
| XM_011528011.1:c.558C>G | XP_011526313.1:p.Cys186Trp | |
| XR_244074.2:n.1089C>G | ||
| XM_011528010.2:c.939C>G | XP_011526312.1:p.Cys313Trp | |
| XR_001753685.2:n.1056C>G | ||
| XR_001753686.2:n.1056C>G | ||
| NM_000527.5:c.939C>G MANE Select | NP_000518.1:p.Cys313Trp | |
| NM_001195798.2:c.939C>G | NP_001182727.1:p.Cys313Trp | |
| NM_001195799.2:c.816C>G | NP_001182728.1:p.Cys272Trp | |
| NM_001195800.2:c.435C>G | NP_001182729.1:p.Cys145Trp | |
| NM_001195803.2:c.558C>G | NP_001182732.1:p.Cys186Trp |