HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665013T>G , CM000679.2:g.39665013T>G | GRCh38 |
NC_000017.10:g.37821266T>G , CM000679.1:g.37821266T>G | GRCh37 |
NC_000017.9:g.35074792T>G | NCBI36 |
NG_008892.1:g.4668T>G , LRG_210:g.4668T>G | |
NG_042278.1:g.2033T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.2:c.-347T>G | ENSP00000312624.2:n.-347T>G |