HGVS | Genome Assembly |
---|---|
NC_000003.12:g.111333471C>T , CM000665.2:g.111333471C>T | GRCh38 |
NC_000003.11:g.111052318C>T , CM000665.1:g.111052318C>T | GRCh37 |
NC_000003.10:g.112535008C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460744.1:c.-325-31042C>T | ENSP00000475194.1:n.-325-31042C>T | |
XR_924332.1:n.163+26953C>T |