HGVS | Genome Assembly |
---|---|
NC_000023.11:g.141895513C= , CM000685.2:g.141895513C= | GRCh38 |
NC_000023.10:g.140983299C= , CM000685.1:g.140983299C= | GRCh37 |
NC_000023.9:g.140810965C= | NCBI36 |
NG_013272.1:g.62198C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000298296.1:c.1077C= MANE Select | ENSP00000298296.1:p.Gly359= | |
ENST00000443323.2:c.-118-918C= | ENSP00000438254.1:n.-118-918C= | |
ENST00000483584.5:n.288+106C= | ||
ENST00000544766.5:c.-240+106C= | ENSP00000440444.1:n.-240+106C= | |
NM_138702.1:c.1077C= MANE Select | NP_619647.1:p.Gly359= | |
NM_177456.2:c.-240+106C= | NP_803251.1:n.-240+106C= | |
XM_011531267.1:c.-163+106C= | XP_011529569.1:n.-163+106C= | |
XM_011531267.3:c.-163+106C= | XP_011529569.1:n.-163+106C= | |
XM_017029265.2:c.-240+106C= | XP_016884754.1:n.-240+106C= |