HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27323173G>C , CM000664.2:g.27323173G>C | GRCh38 |
NC_000002.11:g.27546040G>C , CM000664.1:g.27546040G>C | GRCh37 |
NC_000002.10:g.27399544G>C | NCBI36 |
NG_008075.1:g.4392C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357186.10:c.18+1260C>G | ENSP00000349713.6:n.18+1260C>G | |
XM_005264327.2:c.-251C>G | XP_005264384.1:n.-251C>G |