HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58281033C>T , CM000679.2:g.58281033C>T | GRCh38 |
NC_000017.10:g.56358394C>T , CM000679.1:g.56358394C>T | GRCh37 |
NC_000017.9:g.53713393C>T | NCBI36 |
NG_009629.1:g.4903G>A , LRG_84:g.4903G>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011524821.1:c.107G>A | XP_011523123.1:p.Gly36Glu | |
XM_011524823.1:c.107G>A | XP_011523125.1:p.Gly36Glu |