HGVS | Genome Assembly |
---|---|
NC_000010.11:g.102837133C>A , CM000672.2:g.102837133C>A | GRCh38 |
NC_000010.10:g.104596890C>A , CM000672.1:g.104596890C>A | GRCh37 |
NC_000010.9:g.104586880C>A | NCBI36 |
NG_007955.1:g.5401G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369887.4:c.229G>T MANE Select | ENSP00000358903.3:p.Gly77Cys | |
ENST00000638190.1:c.229G>T | ENSP00000492539.1:p.Gly77Cys | |
ENST00000638272.1:c.229G>T | ENSP00000491508.1:p.Gly77Cys | |
ENST00000638971.1:c.229G>T | ENSP00000492313.1:p.Gly77Cys | |
ENST00000639393.1:c.229G>T | ENSP00000492651.1:p.Gly77Cys | |
ENST00000369887.3:c.229G>T | ENSP00000358903.3:p.Gly77Cys | |
ENST00000489268.1:n.282G>T | ||
NM_000102.3:c.229G>T | NP_000093.1:p.Gly77Cys | |
NM_000102.4:c.229G>T MANE Select | NP_000093.1:p.Gly77Cys |