HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45461932A>T , CM000667.2:g.45461932A>T | GRCh38 |
NC_000005.9:g.45462034A>T , CM000667.1:g.45462034A>T | GRCh37 |
NC_000005.8:g.45497791A>T | NCBI36 |
NG_042183.1:g.239187T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303230.6:c.925T>A MANE Select | ENSP00000307342.4:p.Cys309Ser | |
ENST00000637305.1:n.88T>A | ||
ENST00000673735.1:c.925T>A | ENSP00000501107.1:p.Cys309Ser | |
ENST00000303230.5:c.925T>A | ENSP00000307342.4:p.Cys309Ser | |
NM_021072.3:c.925T>A | NP_066550.2:p.Cys309Ser | |
NM_021072.4:c.925T>A MANE Select | NP_066550.2:p.Cys309Ser |