HGVS | Genome Assembly |
---|---|
NC_000004.12:g.101668126G>T , CM000666.2:g.101668126G>T | GRCh38 |
NC_000004.11:g.102589283G>T , CM000666.1:g.102589283G>T | GRCh37 |
NC_000004.10:g.102808306G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000504592.5:c.-255-1277G>T | ENSP00000421443.1:n.-255-1277G>T |