Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81578084C>A , CM000665.2:g.81578084C>A | GRCh38 |
| NC_000003.11:g.81627235C>A , CM000665.1:g.81627235C>A | GRCh37 |
| NC_000003.10:g.81709925C>A | NCBI36 |
| NG_011810.1:g.188717G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000158.4:c.1459G>T MANE Select | NP_000149.4:p.Asp487Tyr |
| ENST00000429644.7:c.1459G>T MANE Select | ENSP00000410833.2:p.Asp487Tyr |
| NM_000158.3:c.1459G>T | NP_000149.3:p.Asp487Tyr |
| ENST00000429644.6:c.1459G>T | ENSP00000410833.2:p.Asp487Tyr |
| ENST00000489715.1:c.1336G>T | ENSP00000419638.1:p.Asp446Tyr |