HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7454493C>A , CM000679.2:g.7454493C>A | GRCh38 |
NC_000017.10:g.7357812C>A , CM000679.1:g.7357812C>A | GRCh37 |
NC_000017.9:g.7298536C>A | NCBI36 |
NG_008026.1:g.14407C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306071.7:c.1017C>A MANE Select | ENSP00000304290.2:p.Thr339= | |
ENST00000306071.6:c.1017C>A | ENSP00000304290.2:p.Thr339= | |
ENST00000536404.6:c.801C>A | ENSP00000439209.2:p.Thr267= | |
ENST00000570557.5:c.680C>A | ||
ENST00000573209.1:n.1961C>A | ||
ENST00000576360.1:c.654C>A | ENSP00000459092.1:p.Thr218= | |
NM_000747.2:c.1017C>A | NP_000738.2:p.Thr339= | |
NM_000747.3:c.1017C>A MANE Select | NP_000738.2:p.Thr339= |