HGVS | Genome Assembly |
---|---|
NC_000003.12:g.53057080C>A , CM000665.2:g.53057080C>A | GRCh38 |
NC_000003.11:g.53091096C>A , CM000665.1:g.53091096C>A | GRCh37 |
NC_000003.10:g.53066136C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000607203.1:c.318-9841G>T | ||
ENST00000607283.5:c.465-13826G>T | ||
ENST00000607495.5:c.447+20608G>T |