HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431190G>T , CM000663.2:g.229431190G>T | GRCh38 |
NC_000001.10:g.229566937G>T , CM000663.1:g.229566937G>T | GRCh37 |
NC_000001.9:g.227633560G>T | NCBI36 |
NG_006672.1:g.7907C>A , LRG_429:g.7907C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684723.1:c.*309C>A | ENSP00000508084.1:n.*309C>A |