HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24794760A>T , CM000666.2:g.24794760A>T | GRCh38 |
NC_000004.11:g.24796382A>T , CM000666.1:g.24796382A>T | GRCh37 |
NC_000004.10:g.24405480A>T | NCBI36 |
NG_012213.1:g.4298A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000598411.1:c.-17+4658A>T | ENSP00000472134.1:n.-17+4658A>T |