Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232480800C>T , CM000664.2:g.232480800C>T | GRCh38 |
| NC_000002.11:g.233345510C>T , CM000664.1:g.233345510C>T | GRCh37 |
| NC_000002.10:g.233053754C>T | NCBI36 |
| NG_034065.1:g.12060G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004826.4:c.2069G>A MANE Select | NP_004817.2:p.Trp690Ter |
| ENST00000304546.6:c.2069G>A MANE Select | ENSP00000302051.1:p.Trp690Ter |
| NM_001290787.1:c.2063G>A | NP_001277716.1:p.Trp688Ter |
| NM_001290787.2:c.2063G>A | NP_001277716.1:p.Trp688Ter |
| NM_004826.3:c.2069G>A | NP_004817.2:p.Trp690Ter |
| ENST00000304546.5:c.2069G>A | ENSP00000302051.1:p.Trp690Ter |
| ENST00000409941.1:c.2063G>A | ENSP00000386333.1:p.Trp688Ter |
| ENST00000411860.5:c.248G>A | ENSP00000412683.1:p.Trp83Ter |
| ENST00000482346.1:n.2380G>A |