HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24794787C>T , CM000666.2:g.24794787C>T | GRCh38 |
NC_000004.11:g.24796409C>T , CM000666.1:g.24796409C>T | GRCh37 |
NC_000004.10:g.24405507C>T | NCBI36 |
NG_012213.1:g.4325C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000598411.1:c.-17+4685C>T | ENSP00000472134.1:n.-17+4685C>T |