HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7455353G>T , CM000679.2:g.7455353G>T | GRCh38 |
NC_000017.10:g.7358672G>T , CM000679.1:g.7358672G>T | GRCh37 |
NC_000017.9:g.7299396G>T | NCBI36 |
NG_008026.1:g.15267G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306071.7:c.1114G>T MANE Select | ENSP00000304290.2:p.Glu372Ter | |
ENST00000306071.6:c.1114G>T | ENSP00000304290.2:p.Glu372Ter | |
ENST00000536404.6:c.898G>T | ENSP00000439209.2:p.Glu300Ter | |
ENST00000570557.5:c.777G>T | ||
ENST00000573209.1:n.2058G>T | ||
ENST00000576360.1:c.751G>T | ENSP00000459092.1:p.Glu251Ter | |
NM_000747.2:c.1114G>T | NP_000738.2:p.Glu372Ter | |
NM_000747.3:c.1114G>T MANE Select | NP_000738.2:p.Glu372Ter |