HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154075G= , CM000681.2:g.55154075G= | GRCh38 |
NC_000019.9:g.55665443G= , CM000681.1:g.55665443G= | GRCh37 |
NC_000019.8:g.60357255G= | NCBI36 |
NG_007866.2:g.8658C= , LRG_432:g.8658C= | |
NG_011829.2:g.164C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.504C= MANE Select | ENSP00000341838.5:p.Asp168= | |
ENST00000665070.1:c.537C= | ENSP00000499482.1:p.Asp179= | |
ENST00000344887.9:c.504C= | ENSP00000341838.5:p.Asp168= | |
ENST00000585806.5:n.503C= | ||
ENST00000588882.1:c.429C= | ENSP00000466729.1:p.Asp143= | |
ENST00000589864.1:n.332C= | ||
NM_000363.4:c.504C= , LRG_432t1:c.504C= | NP_000354.4:p.Asp168= | |
NM_000363.5:c.504C= MANE Select | NP_000354.4:p.Asp168= |