Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151618228T>A , CM000668.2:g.151618228T>A | GRCh38 |
| NC_000006.11:g.151939363T>A , CM000668.1:g.151939363T>A | GRCh37 |
| NC_000006.10:g.151981056T>A | NCBI36 |
| NG_021198.1:g.129189T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.*81T>A MANE Select | ENSP00000239374.6:n.*81T>A | |
| ENST00000239374.7:c.*81T>A | ENSP00000239374.6:n.*81T>A | |
| NM_025059.3:c.*81T>A | NP_079335.2:n.*81T>A | |
| XM_011536147.1:c.*81T>A | XP_011534449.1:n.*81T>A | |
| XM_011536148.1:c.*81T>A | XP_011534450.1:n.*81T>A | |
| XM_011536147.2:c.*81T>A | XP_011534449.1:n.*81T>A | |
| XM_011536148.2:c.*81T>A | XP_011534450.1:n.*81T>A | |
| NM_025059.4:c.*81T>A MANE Select | NP_079335.2:n.*81T>A |