HGVS | Genome Assembly |
---|---|
NC_000017.11:g.75516185C>A , CM000679.2:g.75516185C>A | GRCh38 |
NC_000017.10:g.73512266C>A , CM000679.1:g.73512266C>A | GRCh37 |
NC_000017.9:g.71023861C>A | NCBI36 |
NG_013041.1:g.4658C>A | |
NG_033152.1:g.4399G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000434205.8:c.-284C>A | ENSP00000406559.4:n.-284C>A | |
ENST00000679370.1:n.242C>A | ||
ENST00000434205.7:c.-284C>A | ENSP00000406559.3:n.-284C>A | |
XM_006721821.2:c.-449C>A | XP_006721884.1:n.-449C>A |