HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81578008A>T , CM000665.2:g.81578008A>T | GRCh38 |
NC_000003.11:g.81627159A>T , CM000665.1:g.81627159A>T | GRCh37 |
NC_000003.10:g.81709849A>T | NCBI36 |
NG_011810.1:g.188793T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000429644.7:c.1535T>A MANE Select | ENSP00000410833.2:p.Val512Asp | |
ENST00000429644.6:c.1535T>A | ENSP00000410833.2:p.Val512Asp | |
ENST00000489715.1:c.1412T>A | ENSP00000419638.1:p.Val471Asp | |
NM_000158.3:c.1535T>A | NP_000149.3:p.Val512Asp | |
NM_000158.4:c.1535T>A MANE Select | NP_000149.4:p.Val512Asp |