HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4911862A>T , CM000674.2:g.4911862A>T | GRCh38 |
NC_000012.11:g.5021028A>T , CM000674.1:g.5021028A>T | GRCh37 |
NC_000012.10:g.4891289A>T | NCBI36 |
NG_011815.1:g.6956A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.484A>T MANE Select | ENSP00000371985.3:p.Ser162Cys | |
ENST00000543874.3:n.105+1390A>T | ||
ENST00000639306.1:c.322A>T | ENSP00000492506.1:p.Ser108Cys | |
ENST00000382545.3:c.484A>T | ENSP00000371985.3:p.Ser162Cys | |
ENST00000541095.1:n.105+1390A>T | ||
ENST00000543874.2:n.96+1390A>T | ||
NM_000217.2:c.484A>T | NP_000208.2:p.Ser162Cys | |
NM_000217.3:c.484A>T MANE Select | NP_000208.2:p.Ser162Cys |