HGVS | Genome Assembly |
---|---|
NC_000011.10:g.637585C>G , CM000673.2:g.637585C>G | GRCh38 |
NC_000011.9:g.637585C>G , CM000673.1:g.637585C>G | GRCh37 |
NC_000011.8:g.627585C>G | NCBI36 |
NG_021241.1:g.5281C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000176183.6:c.281C>G MANE Select | ENSP00000176183.5:p.Ser94Cys | |
ENST00000176183.5:c.281C>G | ENSP00000176183.5:p.Ser94Cys | |
NM_000797.3:c.281C>G | NP_000788.2:p.Ser94Cys | |
NM_000797.4:c.281C>G MANE Select | NP_000788.2:p.Ser94Cys |