HGVS | Genome Assembly |
---|---|
NC_000023.11:g.119930043C>T , CM000685.2:g.119930043C>T | GRCh38 |
NC_000023.10:g.119064006C>T , CM000685.1:g.119064006C>T | GRCh37 |
NC_000023.9:g.118948034C>T | NCBI36 |
NG_021260.1:g.18730G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371410.5:c.1046G>A MANE Select | ENSP00000360464.3:p.Cys349Tyr | |
ENST00000652253.1:c.1042G>A | ||
ENST00000371410.4:c.1046G>A | ENSP00000360464.3:p.Cys349Tyr | |
ENST00000477789.5:n.1974G>A | ||
NM_024528.3:c.1046G>A | NP_078804.2:p.Cys349Tyr | |
XM_017029842.1:c.749G>A | XP_016885331.1:p.Cys250Tyr | |
NM_024528.4:c.1046G>A MANE Select | NP_078804.2:p.Cys349Tyr |