HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32038364G= , CM000668.2:g.32038364G= | GRCh38 |
NC_000006.11:g.32006141G= , CM000668.1:g.32006141G= | GRCh37 |
NC_000006.10:g.32114120G= | NCBI36 |
NG_007941.2:g.5060G= | |
NG_007941.3:g.5060G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000418967.6:c.-59G= | ENSP00000408860.2:n.-59G= | |
ENST00000466779.5:c.-59G= | ENSP00000417321.1:n.-59G= | |
ENST00000486063.5:n.25G= | ||
NM_000500.7:c.-59G= | NP_000491.4:n.-59G= | |
NM_001128590.3:c.-59G= | NP_001122062.3:n.-59G= | |
NM_001368143.1:c.-483G= | NP_001355072.1:n.-483G= | |
NM_001368144.1:c.-393G= | NP_001355073.1:n.-393G= |