HGVS | Genome Assembly |
---|---|
NC_000005.10:g.150155866C>A , CM000667.2:g.150155866C>A | GRCh38 |
NC_000005.9:g.149535429C>A , CM000667.1:g.149535429C>A | GRCh37 |
NC_000005.8:g.149515622C>A | NCBI36 |
NG_023367.1:g.4994G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000523456.1:n.7G>T | ||
XM_005268464.2:c.-622G>T | XP_005268521.1:n.-622G>T | |
XM_011537659.1:c.-943G>T | XP_011535961.1:n.-943G>T |