HGVS | Genome Assembly |
---|---|
NC_000001.11:g.220878397G>A , CM000663.2:g.220878397G>A | GRCh38 |
NC_000001.10:g.221051739G>A , CM000663.1:g.221051739G>A | GRCh37 |
NC_000001.9:g.219118362G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651706.1:c.843-2797G>A | ENSP00000499157.1:n.843-2797G>A | |
NR_046901.1:n.292+1452C>T | ||
XM_011510307.1:c.662C>T | XP_011508609.1:p.Thr221Met |