HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154084C= , CM000681.2:g.55154084C= | GRCh38 |
NC_000019.9:g.55665452C= , CM000681.1:g.55665452C= | GRCh37 |
NC_000019.8:g.60357264C= | NCBI36 |
NG_007866.2:g.8649G= , LRG_432:g.8649G= | |
NG_011829.2:g.155G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.495G= MANE Select | ENSP00000341838.5:p.Glu165= | |
ENST00000665070.1:c.528G= | ENSP00000499482.1:p.Glu176= | |
ENST00000344887.9:c.495G= | ENSP00000341838.5:p.Glu165= | |
ENST00000585806.5:n.494G= | ||
ENST00000588882.1:c.420G= | ENSP00000466729.1:p.Glu140= | |
ENST00000589864.1:n.323G= | ||
NM_000363.4:c.495G= , LRG_432t1:c.495G= | NP_000354.4:p.Glu165= | |
NM_000363.5:c.495G= MANE Select | NP_000354.4:p.Glu165= |