HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4912373T>A , CM000674.2:g.4912373T>A | GRCh38 |
NC_000012.11:g.5021539T>A , CM000674.1:g.5021539T>A | GRCh37 |
NC_000012.10:g.4891800T>A | NCBI36 |
NG_011815.1:g.7467T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.995T>A MANE Select | ENSP00000371985.3:p.Phe332Tyr | |
ENST00000543874.3:n.105+1901T>A | ||
ENST00000639306.1:c.833T>A | ENSP00000492506.1:p.Phe278Tyr | |
ENST00000639680.1:c.76+107T>A | ||
ENST00000382545.3:c.995T>A | ENSP00000371985.3:p.Phe332Tyr | |
ENST00000541095.1:n.105+1901T>A | ||
ENST00000543874.2:n.96+1901T>A | ||
NM_000217.2:c.995T>A | NP_000208.2:p.Phe332Tyr | |
NM_000217.3:c.995T>A MANE Select | NP_000208.2:p.Phe332Tyr |