Linked Data
ClinVar Variation Id:
699805
dbSNP Id:
rs1286110371
gnomAD v2:
19-11217263-C-T
gnomAD v3:
19-11106587-C-T
gnomAD v4:
19-11106587-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11106587C>T , CM000681.2:g.11106587C>T | GRCh38 |
| NC_000019.9:g.11217263C>T , CM000681.1:g.11217263C>T | GRCh37 |
| NC_000019.8:g.11078263C>T | NCBI36 |
| NG_009060.1:g.22207C>T , LRG_274:g.22207C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.975C>T | ENSP00000252444.6:p.Asp325= | |
| ENST00000559340.2:c.717C>T | ENSP00000453696.2:p.Asp239= | |
| ENST00000560467.2:c.717C>T | ENSP00000453513.2:p.Asp239= | |
| ENST00000558518.6:c.717C>T MANE Select | ENSP00000454071.1:p.Asp239= | |
| ENST00000252444.9:c.971C>T | ||
| ENST00000455727.6:c.314-805C>T | ENSP00000397829.2:n.314-805C>T | |
| ENST00000535915.5:c.594C>T | ENSP00000440520.1:p.Asp198= | |
| ENST00000545707.5:c.336C>T | ENSP00000437639.1:p.Asp112= | |
| ENST00000557933.5:c.717C>T | ENSP00000453557.1:p.Asp239= | |
| ENST00000558013.5:c.717C>T | ENSP00000453346.1:p.Asp239= | |
| ENST00000558518.5:c.717C>T | ENSP00000454071.1:p.Asp239= | |
| ENST00000558528.1:n.232C>T | ||
| ENST00000560467.1:c.317C>T | ||
| NM_000527.4:c.717C>T , LRG_274t1:c.717C>T | NP_000518.1:p.Asp239= | |
| NM_001195798.1:c.717C>T | NP_001182727.1:p.Asp239= | |
| NM_001195799.1:c.594C>T | NP_001182728.1:p.Asp198= | |
| NM_001195800.1:c.314-805C>T | NP_001182729.1:n.314-805C>T | |
| NM_001195803.1:c.336C>T | NP_001182732.1:p.Asp112= | |
| XM_011528010.1:c.717C>T | XP_011526312.1:p.Asp239= | |
| XM_011528011.1:c.336C>T | XP_011526313.1:p.Asp112= | |
| XR_244074.2:n.867C>T | ||
| XM_011528010.2:c.717C>T | XP_011526312.1:p.Asp239= | |
| XR_001753685.2:n.834C>T | ||
| XR_001753686.2:n.834C>T | ||
| NM_000527.5:c.717C>T MANE Select | NP_000518.1:p.Asp239= | |
| NM_001195798.2:c.717C>T | NP_001182727.1:p.Asp239= | |
| NM_001195799.2:c.594C>T | NP_001182728.1:p.Asp198= | |
| NM_001195800.2:c.314-805C>T | NP_001182729.1:n.314-805C>T | |
| NM_001195803.2:c.336C>T | NP_001182732.1:p.Asp112= |