HGVS | Genome Assembly |
---|---|
NC_000003.12:g.111333850A>T , CM000665.2:g.111333850A>T | GRCh38 |
NC_000003.11:g.111052697A>T , CM000665.1:g.111052697A>T | GRCh37 |
NC_000003.10:g.112535387A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460744.1:c.-325-30663A>T | ENSP00000475194.1:n.-325-30663A>T | |
XR_924332.1:n.163+27332A>T |