HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138946295T= , CM000665.2:g.138946295T= | GRCh38 |
NC_000003.11:g.138665137T= , CM000665.1:g.138665137T= | GRCh37 |
NC_000003.10:g.140147827T= | NCBI36 |
NG_012454.1:g.5846A= | |
NG_029796.1:g.4062T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.428A= MANE Select | ENSP00000497217.1:p.Tyr143= | |
ENST00000330315.3:c.428A= | ENSP00000333188.3:p.Tyr143= | |
NM_023067.3:c.428A= | NP_075555.1:p.Tyr143= | |
NM_023067.4:c.428A= MANE Select | NP_075555.1:p.Tyr143= |