Linked Data
ClinVar Variation Id:
161278
dbSNP Id:
rs5928
ExAC:
19:11240240 G / A
gnomAD v2:
19-11240240-G-A
gnomAD v3:
19-11129564-G-A
gnomAD v4:
19-11129564-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11129564G>A , CM000681.2:g.11129564G>A | GRCh38 |
| NC_000019.9:g.11240240G>A , CM000681.1:g.11240240G>A | GRCh37 |
| NC_000019.8:g.11101240G>A | NCBI36 |
| NG_009060.1:g.45184G>A , LRG_274:g.45184G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2699G>A | ENSP00000252444.6:p.Arg900Gln | |
| ENST00000559340.2:c.*510G>A | ENSP00000453696.2:n.*510G>A | |
| ENST00000560467.2:c.2321G>A | ENSP00000453513.2:p.Arg774Gln | |
| ENST00000558518.6:c.2441G>A MANE Select | ENSP00000454071.1:p.Arg814Gln | |
| ENST00000252444.9:c.2695G>A | ||
| ENST00000455727.6:c.1937G>A | ENSP00000397829.2:p.Arg646Gln | |
| ENST00000535915.5:c.2318G>A | ENSP00000440520.1:p.Arg773Gln | |
| ENST00000545707.5:c.1907G>A | ENSP00000437639.1:p.Arg636Gln | |
| ENST00000557933.5:c.2503G>A | ENSP00000453557.1:p.Gly835Ser | |
| ENST00000558013.5:c.2441G>A | ENSP00000453346.1:p.Arg814Gln | |
| ENST00000558518.5:c.2441G>A | ENSP00000454071.1:p.Arg814Gln | |
| ENST00000560628.1:n.108+1910G>A | ||
| NM_000527.4:c.2441G>A , LRG_274t1:c.2441G>A | NP_000518.1:p.Arg814Gln | |
| NM_001195798.1:c.2441G>A | NP_001182727.1:p.Arg814Gln | |
| NM_001195799.1:c.2318G>A | NP_001182728.1:p.Arg773Gln | |
| NM_001195800.1:c.1937G>A | NP_001182729.1:p.Arg646Gln | |
| NM_001195803.1:c.1907G>A | NP_001182732.1:p.Arg636Gln | |
| XM_011528010.1:c.2363G>A | XP_011526312.1:p.Arg788Gln | |
| XM_011528011.1:c.2060G>A | XP_011526313.1:p.Arg687Gln | |
| XR_244074.2:n.2451G>A | ||
| XM_011528010.2:c.2363G>A | XP_011526312.1:p.Arg788Gln | |
| XR_001753685.2:n.2775G>A | ||
| XR_001753686.2:n.2418G>A | ||
| NM_000527.5:c.2441G>A MANE Select | NP_000518.1:p.Arg814Gln | |
| NM_001195798.2:c.2441G>A | NP_001182727.1:p.Arg814Gln | |
| NM_001195799.2:c.2318G>A | NP_001182728.1:p.Arg773Gln | |
| NM_001195800.2:c.1937G>A | NP_001182729.1:p.Arg646Gln | |
| NM_001195803.2:c.1907G>A | NP_001182732.1:p.Arg636Gln |