HGVS | Genome Assembly |
---|---|
NC_000001.11:g.173208097C>A , CM000663.2:g.173208097C>A | GRCh38 |
NC_000001.10:g.173177236C>A , CM000663.1:g.173177236C>A | GRCh37 |
NC_000001.9:g.171443859C>A | NCBI36 |
NG_011477.1:g.4236G>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_011509964.2:c.148G>T | XP_011508266.2:p.Asp50Tyr | |
XM_017002229.1:c.25-912G>T | XP_016857718.1:n.25-912G>T | |
XM_017002230.1:c.19-912G>T | XP_016857719.1:n.19-912G>T |