HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94041250G= , CM000663.2:g.94041250G= | GRCh38 |
NC_000001.10:g.94506806G= , CM000663.1:g.94506806G= | GRCh37 |
NC_000001.9:g.94279394G= | NCBI36 |
NG_009073.1:g.84900C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.3481C= MANE Select | ENSP00000359245.3:p.Arg1161= | |
ENST00000370225.3:c.3481C= | ENSP00000359245.3:p.Arg1161= | |
ENST00000536513.5:c.-64-1161C= | ENSP00000439707.2:n.-64-1161C= | |
NM_000350.2:c.3481C= | NP_000341.2:p.Arg1161= | |
NM_000350.3:c.3481C= MANE Select | NP_000341.2:p.Arg1161= |