Canonical Allele Identifier: CA363503963
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039605C>G , CM000668.2:g.32039605C>G GRCh38
NC_000006.11:g.32007382C>G , CM000668.1:g.32007382C>G GRCh37
NC_000006.10:g.32115361C>G NCBI36
NG_007941.2:g.6298C>G
NG_008337.2:g.74770G>C
NG_007941.3:g.6301C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.609C>G MANE Select ENSP00000496625.1:p.Ser203Arg
ENST00000418967.6:c.609C>G ENSP00000408860.2:p.Ser203Arg
ENST00000435122.3:c.519C>G ENSP00000415043.2:p.Ser173Arg
ENST00000462278.1:n.197C>G
ENST00000464325.5:n.530C>G
ENST00000466779.5:c.*301C>G ENSP00000417321.1:n.*301C>G
ENST00000466879.5:n.660C>G
ENST00000469053.5:c.*301C>G ENSP00000418104.1:n.*301C>G
ENST00000471671.4:c.570C>G ENSP00000418561.1:p.Ser190Arg
ENST00000479074.5:n.667C>G
ENST00000479730.5:n.725C>G
ENST00000483041.5:n.778C>G
ENST00000486063.5:n.789C>G
NM_000500.7:c.609C>G NP_000491.4:p.Ser203Arg
NM_001128590.3:c.519C>G NP_001122062.3:p.Ser173Arg
XM_011514314.1:c.204C>G XP_011512616.1:p.Ser68Arg
NM_000500.9:c.609C>G MANE Select NP_000491.4:p.Ser203Arg
NM_001368143.1:c.204C>G NP_001355072.1:p.Ser68Arg
NM_001368144.1:c.204C>G NP_001355073.1:p.Ser68Arg
NM_001128590.4:c.519C>G NP_001122062.3:p.Ser173Arg
NM_001368143.2:c.204C>G NP_001355072.1:p.Ser68Arg
NM_001368144.2:c.204C>G NP_001355073.1:p.Ser68Arg