Linked Data
ClinVar Variation Id:
440624
dbSNP Id:
rs749322464
ExAC:
19:11222209 T / G
gnomAD v2:
19-11222209-T-G
gnomAD v3:
19-11111533-T-G
gnomAD v4:
19-11111533-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11111533T>G , CM000681.2:g.11111533T>G | GRCh38 |
| NC_000019.9:g.11222209T>G , CM000681.1:g.11222209T>G | GRCh37 |
| NC_000019.8:g.11083209T>G | NCBI36 |
| NG_009060.1:g.27153T>G , LRG_274:g.27153T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1338T>G | ENSP00000252444.6:p.Asp446Glu | |
| ENST00000559340.2:c.1080T>G | ENSP00000453696.2:p.Asp360Glu | |
| ENST00000560467.2:c.960T>G | ENSP00000453513.2:p.Asp320Glu | |
| ENST00000558518.6:c.1080T>G MANE Select | ENSP00000454071.1:p.Asp360Glu | |
| ENST00000252444.9:c.1334T>G | ||
| ENST00000455727.6:c.576T>G | ENSP00000397829.2:p.Asp192Glu | |
| ENST00000535915.5:c.957T>G | ENSP00000440520.1:p.Asp319Glu | |
| ENST00000545707.5:c.699T>G | ENSP00000437639.1:p.Asp233Glu | |
| ENST00000557933.5:c.1080T>G | ENSP00000453557.1:p.Asp360Glu | |
| ENST00000558013.5:c.1080T>G | ENSP00000453346.1:p.Asp360Glu | |
| ENST00000558518.5:c.1080T>G | ENSP00000454071.1:p.Asp360Glu | |
| ENST00000560173.1:n.79T>G | ||
| ENST00000560467.1:c.560T>G | ||
| NM_000527.4:c.1080T>G , LRG_274t1:c.1080T>G | NP_000518.1:p.Asp360Glu | |
| NM_001195798.1:c.1080T>G | NP_001182727.1:p.Asp360Glu | |
| NM_001195799.1:c.957T>G | NP_001182728.1:p.Asp319Glu | |
| NM_001195800.1:c.576T>G | NP_001182729.1:p.Asp192Glu | |
| NM_001195803.1:c.699T>G | NP_001182732.1:p.Asp233Glu | |
| XM_011528010.1:c.1080T>G | XP_011526312.1:p.Asp360Glu | |
| XM_011528011.1:c.699T>G | XP_011526313.1:p.Asp233Glu | |
| XR_244074.2:n.1230T>G | ||
| XM_011528010.2:c.1080T>G | XP_011526312.1:p.Asp360Glu | |
| XR_001753685.2:n.1197T>G | ||
| XR_001753686.2:n.1197T>G | ||
| NM_000527.5:c.1080T>G MANE Select | NP_000518.1:p.Asp360Glu | |
| NM_001195798.2:c.1080T>G | NP_001182727.1:p.Asp360Glu | |
| NM_001195799.2:c.957T>G | NP_001182728.1:p.Asp319Glu | |
| NM_001195800.2:c.576T>G | NP_001182729.1:p.Asp192Glu | |
| NM_001195803.2:c.699T>G | NP_001182732.1:p.Asp233Glu |