Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659477T>A , CM000665.2:g.180659477T>A | GRCh38 |
| NC_000003.11:g.180377265T>A , CM000665.1:g.180377265T>A | GRCh37 |
| NC_000003.10:g.181859959T>A | NCBI36 |
| NG_029581.1:g.25019A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.713A>T MANE Select | ENSP00000417960.2:p.Asp238Val | |
| ENST00000650641.1:n.792A>T | ||
| ENST00000650889.1:n.885A>T | ||
| ENST00000651046.1:c.713A>T | ENSP00000499175.1:p.Asp238Val | |
| ENST00000651818.1:n.855A>T | ||
| ENST00000652024.1:n.804A>T | ||
| ENST00000652408.1:n.850A>T | ||
| ENST00000442201.6:c.713A>T | ENSP00000405708.2:p.Asp238Val | |
| ENST00000476379.5:c.713A>T | ENSP00000417960.1:p.Asp238Val | |
| NM_181426.1:c.713A>T | NP_852091.1:p.Asp238Val | |
| NM_181426.2:c.713A>T MANE Select | NP_852091.1:p.Asp238Val |