HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24794992C>T , CM000666.2:g.24794992C>T | GRCh38 |
NC_000004.11:g.24796614C>T , CM000666.1:g.24796614C>T | GRCh37 |
NC_000004.10:g.24405712C>T | NCBI36 |
NG_012213.1:g.4530C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000598411.1:c.-16-4514C>T | ENSP00000472134.1:n.-16-4514C>T |