Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911983T>A , CM000674.2:g.4911983T>A | GRCh38 |
| NC_000012.11:g.5021149T>A , CM000674.1:g.5021149T>A | GRCh37 |
| NC_000012.10:g.4891410T>A | NCBI36 |
| NG_011815.1:g.7077T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.605T>A MANE Select | ENSP00000371985.3:p.Val202Asp | |
| ENST00000543874.3:n.105+1511T>A | ||
| ENST00000639306.1:c.443T>A | ENSP00000492506.1:p.Val148Asp | |
| ENST00000382545.3:c.605T>A | ENSP00000371985.3:p.Val202Asp | |
| ENST00000541095.1:n.105+1511T>A | ||
| ENST00000543874.2:n.96+1511T>A | ||
| NM_000217.2:c.605T>A | NP_000208.2:p.Val202Asp | |
| NM_000217.3:c.605T>A MANE Select | NP_000208.2:p.Val202Asp |