HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7455888T>A , CM000679.2:g.7455888T>A | GRCh38 |
NC_000017.10:g.7359207T>A , CM000679.1:g.7359207T>A | GRCh37 |
NC_000017.9:g.7299931T>A | NCBI36 |
NG_008026.1:g.15802T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306071.7:c.1312T>A MANE Select | ENSP00000304290.2:p.Ser438Thr | |
ENST00000306071.6:c.1312T>A | ENSP00000304290.2:p.Ser438Thr | |
ENST00000536404.6:c.1096T>A | ENSP00000439209.2:p.Ser366Thr | |
ENST00000575379.1:c.-81T>A | ENSP00000461751.1:n.-81T>A | |
ENST00000576360.1:c.949T>A | ENSP00000459092.1:p.Ser317Thr | |
NM_000747.2:c.1312T>A | NP_000738.2:p.Ser438Thr | |
NM_000747.3:c.1312T>A MANE Select | NP_000738.2:p.Ser438Thr |