HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10115558G>A , CM000681.2:g.10115558G>A | GRCh38 |
NC_000019.9:g.10226234G>A , CM000681.1:g.10226234G>A | GRCh37 |
NC_000019.8:g.10087234G>A | NCBI36 |
NG_047007.1:g.9038G>A | |
NG_051197.1:g.9367C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253108.9:c.868C>T MANE Select | ENSP00000253108.3:p.Arg290Cys | |
ENST00000253108.8:c.868C>T | ENSP00000253108.3:p.Arg290Cys | |
ENST00000589454.5:c.844C>T | ENSP00000466860.1:p.Arg282Cys | |
ENST00000590158.1:n.887C>T | ||
ENST00000593054.5:c.262C>T | ENSP00000467187.1:p.Arg88Cys | |
NM_003755.3:c.868C>T | NP_003746.2:p.Arg290Cys | |
NM_003755.4:c.868C>T | NP_003746.2:p.Arg290Cys | |
NM_003755.5:c.868C>T MANE Select | NP_003746.2:p.Arg290Cys |