HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58281555C>A , CM000679.2:g.58281555C>A | GRCh38 |
NC_000017.10:g.56358916C>A , CM000679.1:g.56358916C>A | GRCh37 |
NC_000017.9:g.53713915C>A | NCBI36 |
NG_009629.1:g.4381G>T , LRG_84:g.4381G>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_011524821.1:c.71-486G>T | XP_011523123.1:n.71-486G>T | |
XM_011524823.1:c.71-486G>T | XP_011523125.1:n.71-486G>T |