HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32038356A>G , CM000668.2:g.32038356A>G | GRCh38 |
NC_000006.11:g.32006133A>G , CM000668.1:g.32006133A>G | GRCh37 |
NC_000006.10:g.32114112A>G | NCBI36 |
NG_007941.2:g.5052A>G | |
NG_007941.3:g.5052A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000418967.6:c.-67A>G | ENSP00000408860.2:n.-67A>G | |
ENST00000466779.5:c.-67A>G | ENSP00000417321.1:n.-67A>G | |
ENST00000486063.5:n.17A>G | ||
NM_000500.7:c.-67A>G | NP_000491.4:n.-67A>G | |
NM_001128590.3:c.-67A>G | NP_001122062.3:n.-67A>G | |
NM_001368143.1:c.-491A>G | NP_001355072.1:n.-491A>G | |
NM_001368144.1:c.-401A>G | NP_001355073.1:n.-401A>G |