Linked Data
ClinVar Variation Id:
251778
dbSNP Id:
rs779732323
ExAC:
19:11224074 T / C
gnomAD v2:
19-11224074-T-C
gnomAD v3:
19-11113398-T-C
gnomAD v4:
19-11113398-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11113398T>C , CM000681.2:g.11113398T>C | GRCh38 |
| NC_000019.9:g.11224074T>C , CM000681.1:g.11224074T>C | GRCh37 |
| NC_000019.8:g.11085074T>C | NCBI36 |
| NG_009060.1:g.29018T>C , LRG_274:g.29018T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1565T>C | ENSP00000252444.6:p.Val522Ala | |
| ENST00000559340.2:c.1307T>C | ENSP00000453696.2:p.Val436Ala | |
| ENST00000560467.2:c.1187T>C | ENSP00000453513.2:p.Val396Ala | |
| ENST00000558518.6:c.1307T>C MANE Select | ENSP00000454071.1:p.Val436Ala | |
| ENST00000252444.9:c.1561T>C | ||
| ENST00000455727.6:c.803T>C | ENSP00000397829.2:p.Val268Ala | |
| ENST00000535915.5:c.1184T>C | ENSP00000440520.1:p.Val395Ala | |
| ENST00000545707.5:c.926T>C | ENSP00000437639.1:p.Val309Ala | |
| ENST00000557933.5:c.1307T>C | ENSP00000453557.1:p.Val436Ala | |
| ENST00000558013.5:c.1307T>C | ENSP00000453346.1:p.Val436Ala | |
| ENST00000558518.5:c.1307T>C | ENSP00000454071.1:p.Val436Ala | |
| ENST00000559340.1:c.28T>C | ||
| ENST00000560173.1:n.306T>C | ||
| ENST00000560467.1:c.787T>C | ||
| NM_000527.4:c.1307T>C , LRG_274t1:c.1307T>C | NP_000518.1:p.Val436Ala | |
| NM_001195798.1:c.1307T>C | NP_001182727.1:p.Val436Ala | |
| NM_001195799.1:c.1184T>C | NP_001182728.1:p.Val395Ala | |
| NM_001195800.1:c.803T>C | NP_001182729.1:p.Val268Ala | |
| NM_001195803.1:c.926T>C | NP_001182732.1:p.Val309Ala | |
| XM_011528010.1:c.1307T>C | XP_011526312.1:p.Val436Ala | |
| XM_011528011.1:c.926T>C | XP_011526313.1:p.Val309Ala | |
| XR_244074.2:n.1457T>C | ||
| XM_011528010.2:c.1307T>C | XP_011526312.1:p.Val436Ala | |
| XR_001753685.2:n.1424T>C | ||
| XR_001753686.2:n.1424T>C | ||
| NM_000527.5:c.1307T>C MANE Select | NP_000518.1:p.Val436Ala | |
| NM_001195798.2:c.1307T>C | NP_001182727.1:p.Val436Ala | |
| NM_001195799.2:c.1184T>C | NP_001182728.1:p.Val395Ala | |
| NM_001195800.2:c.803T>C | NP_001182729.1:p.Val268Ala | |
| NM_001195803.2:c.926T>C | NP_001182732.1:p.Val309Ala |