HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670664T>C , CM000666.2:g.68670664T>C | GRCh38 |
NC_000004.11:g.69536382T>C , CM000666.1:g.69536382T>C | GRCh37 |
NC_000004.10:g.69218977T>C | NCBI36 |
NG_052676.1:g.5113A>G |
HGVS | Amino-acid Change | |
---|---|---|
NM_001076.3:c.-46A>G | NP_001067.2:n.-46A>G |