Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232480401G>A , CM000664.2:g.232480401G>A | GRCh38 |
| NC_000002.11:g.233345111G>A , CM000664.1:g.233345111G>A | GRCh37 |
| NC_000002.10:g.233053355G>A | NCBI36 |
| NG_034065.1:g.12459C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304546.6:c.2226C>T MANE Select | ENSP00000302051.1:p.Tyr742= | |
| ENST00000304546.5:c.2226C>T | ENSP00000302051.1:p.Tyr742= | |
| ENST00000409941.1:c.2220C>T | ENSP00000386333.1:p.Tyr740= | |
| ENST00000411860.5:c.405C>T | ENSP00000412683.1:p.Tyr135= | |
| ENST00000482346.1:n.2537C>T | ||
| NM_001290787.1:c.2220C>T | NP_001277716.1:p.Tyr740= | |
| NM_004826.3:c.2226C>T | NP_004817.2:p.Tyr742= | |
| NM_004826.4:c.2226C>T MANE Select | NP_004817.2:p.Tyr742= | |
| NM_001290787.2:c.2220C>T | NP_001277716.1:p.Tyr740= |