HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118304577A>T , CM000673.2:g.118304577A>T | GRCh38 |
NC_000011.9:g.118175292A>T , CM000673.1:g.118175292A>T | GRCh37 |
NC_000011.8:g.117680502A>T | NCBI36 |
NG_007383.1:g.4998A>T , LRG_38:g.4998A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.8:c.-259A>T | ENSP00000354566.4:n.-259A>T |