HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24794799A>G , CM000666.2:g.24794799A>G | GRCh38 |
NC_000004.11:g.24796421A>G , CM000666.1:g.24796421A>G | GRCh37 |
NC_000004.10:g.24405519A>G | NCBI36 |
NG_012213.1:g.4337A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000598411.1:c.-17+4697A>G | ENSP00000472134.1:n.-17+4697A>G |