HGVS | Genome Assembly |
---|---|
NC_000017.11:g.75516140G>A , CM000679.2:g.75516140G>A | GRCh38 |
NC_000017.10:g.73512221G>A , CM000679.1:g.73512221G>A | GRCh37 |
NC_000017.9:g.71023816G>A | NCBI36 |
NG_013041.1:g.4613G>A | |
NG_033152.1:g.4444C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000434205.8:c.-329G>A | ENSP00000406559.4:n.-329G>A | |
ENST00000679370.1:n.197G>A | ||
ENST00000434205.7:c.-329G>A | ENSP00000406559.3:n.-329G>A | |
XM_006721821.2:c.-494G>A | XP_006721884.1:n.-494G>A |