HGVS | Genome Assembly |
---|---|
NC_000003.12:g.72388262C>A , CM000665.2:g.72388262C>A | GRCh38 |
NC_000003.11:g.72437413C>A , CM000665.1:g.72437413C>A | GRCh37 |
NC_000003.10:g.72520103C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000477973.5:c.127-8835G>T | ||
ENST00000477973.4:c.129-8835G>T | ENSP00000419494.3:n.129-8835G>T | |
ENST00000477973.2:c.424-8835G>T |