HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2340767C>G , CM000678.2:g.2340767C>G | GRCh38 |
NC_000016.9:g.2390768C>G , CM000678.1:g.2390768C>G | GRCh37 |
NC_000016.8:g.2330769C>G | NCBI36 |
NG_011790.1:g.4980G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000640929.1:n.42+1436C>G | ||
ENST00000512848.5:n.182+1436C>G |