HGVS | Genome Assembly |
---|---|
NC_000007.14:g.99161494C>A , CM000669.2:g.99161494C>A | GRCh38 |
NC_000007.13:g.98759117C>A , CM000669.1:g.98759117C>A | GRCh37 |
NC_000007.12:g.98597053C>A | NCBI36 |
NG_051213.1:g.62924G>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_017012211.1:c.1546-15178G>T | XP_016867700.1:n.1546-15178G>T |