HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55346161C>A , CM000666.2:g.55346161C>A | GRCh38 |
NC_000004.11:g.56212328C>A , CM000666.1:g.56212328C>A | GRCh37 |
NC_000004.10:g.55907085C>A | NCBI36 |
NG_028230.1:g.4941C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264228.8:c.-176C>A | ENSP00000264228.4:n.-176C>A |