HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24795013C>G , CM000666.2:g.24795013C>G | GRCh38 |
NC_000004.11:g.24796635C>G , CM000666.1:g.24796635C>G | GRCh37 |
NC_000004.10:g.24405733C>G | NCBI36 |
NG_012213.1:g.4551C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000598411.1:c.-16-4493C>G | ENSP00000472134.1:n.-16-4493C>G |