HGVS | Genome Assembly |
---|---|
NC_000017.11:g.75516174G>T , CM000679.2:g.75516174G>T | GRCh38 |
NC_000017.10:g.73512255G>T , CM000679.1:g.73512255G>T | GRCh37 |
NC_000017.9:g.71023850G>T | NCBI36 |
NG_013041.1:g.4647G>T | |
NG_033152.1:g.4410C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000434205.8:c.-295G>T | ENSP00000406559.4:n.-295G>T | |
ENST00000679370.1:n.231G>T | ||
ENST00000434205.7:c.-295G>T | ENSP00000406559.3:n.-295G>T | |
XM_006721821.2:c.-460G>T | XP_006721884.1:n.-460G>T |