HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81578003C>A , CM000665.2:g.81578003C>A | GRCh38 |
NC_000003.11:g.81627154C>A , CM000665.1:g.81627154C>A | GRCh37 |
NC_000003.10:g.81709844C>A | NCBI36 |
NG_011810.1:g.188798G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000429644.7:c.1540G>T MANE Select | ENSP00000410833.2:p.Asp514Tyr | |
ENST00000429644.6:c.1540G>T | ENSP00000410833.2:p.Asp514Tyr | |
ENST00000489715.1:c.1417G>T | ENSP00000419638.1:p.Asp473Tyr | |
NM_000158.3:c.1540G>T | NP_000149.3:p.Asp514Tyr | |
NM_000158.4:c.1540G>T MANE Select | NP_000149.4:p.Asp514Tyr |