HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190319T>C , CM000663.2:g.204190319T>C | GRCh38 |
NC_000001.10:g.204159447T>C , CM000663.1:g.204159447T>C | GRCh37 |
NC_000001.9:g.202426070T>C | NCBI36 |
NG_032151.1:g.11173A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000638118.1:c.-298A>G | ENSP00000490307.1:n.-298A>G |