HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118304559A>T , CM000673.2:g.118304559A>T | GRCh38 |
NC_000011.9:g.118175274A>T , CM000673.1:g.118175274A>T | GRCh37 |
NC_000011.8:g.117680484A>T | NCBI36 |
NG_007383.1:g.4980A>T , LRG_38:g.4980A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.8:c.-277A>T | ENSP00000354566.4:n.-277A>T |