HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586913G>C , CM000679.2:g.41586913G>C | GRCh38 |
NC_000017.10:g.39743165G>C , CM000679.1:g.39743165G>C | GRCh37 |
NC_000017.9:g.36996691G>C | NCBI36 |
NG_008624.1:g.4983C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.6:c.-79C>G | ENSP00000167586.6:n.-79C>G |