HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24794871T>A , CM000666.2:g.24794871T>A | GRCh38 |
NC_000004.11:g.24796493T>A , CM000666.1:g.24796493T>A | GRCh37 |
NC_000004.10:g.24405591T>A | NCBI36 |
NG_012213.1:g.4409T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000598411.1:c.-16-4635T>A | ENSP00000472134.1:n.-16-4635T>A |