Linked Data
dbSNP Id:
rs371482223
ExAC:
19:11231162 A / G
gnomAD v2:
19-11231162-A-G
gnomAD v4:
19-11120486-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11120486A>G , CM000681.2:g.11120486A>G | GRCh38 |
| NC_000019.9:g.11231162A>G , CM000681.1:g.11231162A>G | GRCh37 |
| NC_000019.8:g.11092162A>G | NCBI36 |
| NG_009060.1:g.36106A>G , LRG_274:g.36106A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2362A>G | ENSP00000252444.6:p.Met788Val | |
| ENST00000559340.2:c.*173A>G | ENSP00000453696.2:n.*173A>G | |
| ENST00000560467.2:c.1984A>G | ENSP00000453513.2:p.Met662Val | |
| ENST00000558518.6:c.2104A>G MANE Select | ENSP00000454071.1:p.Met702Val | |
| ENST00000252444.9:c.2358A>G | ||
| ENST00000455727.6:c.1600A>G | ENSP00000397829.2:p.Met534Val | |
| ENST00000535915.5:c.1981A>G | ENSP00000440520.1:p.Met661Val | |
| ENST00000545707.5:c.1606+253A>G | ENSP00000437639.1:n.1606+253A>G | |
| ENST00000557933.5:c.2104A>G | ENSP00000453557.1:p.Met702Val | |
| ENST00000558013.5:c.2104A>G | ENSP00000453346.1:p.Met702Val | |
| ENST00000558518.5:c.2104A>G | ENSP00000454071.1:p.Met702Val | |
| NM_000527.4:c.2104A>G , LRG_274t1:c.2104A>G | NP_000518.1:p.Met702Val | |
| NM_001195798.1:c.2104A>G | NP_001182727.1:p.Met702Val | |
| NM_001195799.1:c.1981A>G | NP_001182728.1:p.Met661Val | |
| NM_001195800.1:c.1600A>G | NP_001182729.1:p.Met534Val | |
| NM_001195803.1:c.1606+253A>G | NP_001182732.1:n.1606+253A>G | |
| XM_011528010.1:c.2104A>G | XP_011526312.1:p.Met702Val | |
| XM_011528011.1:c.1723A>G | XP_011526313.1:p.Met575Val | |
| XR_244074.2:n.2114A>G | ||
| XM_011528010.2:c.2104A>G | XP_011526312.1:p.Met702Val | |
| XR_001753685.2:n.2221A>G | ||
| XR_001753686.2:n.2081A>G | ||
| NM_000527.5:c.2104A>G MANE Select | NP_000518.1:p.Met702Val | |
| NM_001195798.2:c.2104A>G | NP_001182727.1:p.Met702Val | |
| NM_001195799.2:c.1981A>G | NP_001182728.1:p.Met661Val | |
| NM_001195800.2:c.1600A>G | NP_001182729.1:p.Met534Val | |
| NM_001195803.2:c.1606+253A>G | NP_001182732.1:n.1606+253A>G |