HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99353038C>A , CM000666.2:g.99353038C>A | GRCh38 |
NC_000004.11:g.100274195C>A , CM000666.1:g.100274195C>A | GRCh37 |
NC_000004.10:g.100493218C>A | NCBI36 |
NG_011718.1:g.4723G>T |
HGVS | Amino-acid Change | |
---|---|---|
NM_000669.4:c.-363G>T | NP_000660.1:n.-363G>T | |
NR_133005.1:n.8G>T | ||
XM_011531589.1:c.-603G>T | XP_011529891.1:n.-603G>T |