Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.185146906G>A , CM000666.2:g.185146906G>A | GRCh38 |
| NC_000004.11:g.186068060G>A , CM000666.1:g.186068060G>A | GRCh37 |
| NC_000004.10:g.186305054G>A | NCBI36 |
| NG_013001.1:g.8644G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001151.4:c.832G>A MANE Select | NP_001142.2:p.Val278Met |
| ENST00000281456.11:c.832G>A MANE Select | ENSP00000281456.5:p.Val278Met |
| NM_001151.3:c.832G>A | NP_001142.2:p.Val278Met |
| ENST00000281456.10:c.832G>A | ENSP00000281456.5:p.Val278Met |
| ENST00000491736.1:c.*609G>A | ENSP00000476711.1:n.*609G>A |