Canonical Allele Identifier: CA2678089992

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040823-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040823C>G , CM000668.2:g.32040823C>G	GRCh38
NC_000006.11:g.32008600C>G , CM000668.1:g.32008600C>G	GRCh37
NC_000006.10:g.32116579C>G	NCBI36
NG_007941.2:g.7516C>G
NG_008337.2:g.73552G>C
NG_007941.3:g.7519C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1223-46C>G MANE Select	ENSP00000496625.1:n.1223-46C>G
ENST00000418967.6:c.1223-46C>G	ENSP00000408860.2:n.1223-46C>G
ENST00000435122.3:c.1133-46C>G	ENSP00000415043.2:n.1133-46C>G
ENST00000479074.5:n.1364-46C>G
ENST00000479730.5:n.1339-46C>G
ENST00000483041.5:n.1392-46C>G
ENST00000486063.5:n.1202-46C>G
NM_000500.7:c.1223-46C>G	NP_000491.4:n.1223-46C>G
NM_001128590.3:c.1133-46C>G	NP_001122062.3:n.1133-46C>G
XM_011514314.1:c.818-46C>G	XP_011512616.1:n.818-46C>G
NM_000500.9:c.1223-46C>G MANE Select	NP_000491.4:n.1223-46C>G
NM_001368143.1:c.818-46C>G	NP_001355072.1:n.818-46C>G
NM_001368144.1:c.818-46C>G	NP_001355073.1:n.818-46C>G
NM_001128590.4:c.1133-46C>G	NP_001122062.3:n.1133-46C>G
NM_001368143.2:c.818-46C>G	NP_001355072.1:n.818-46C>G
NM_001368144.2:c.818-46C>G	NP_001355073.1:n.818-46C>G