Canonical Allele Identifier: CA2678089124

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040322-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040322A>G , CM000668.2:g.32040322A>G	GRCh38
NC_000006.11:g.32008099A>G , CM000668.1:g.32008099A>G	GRCh37
NC_000006.10:g.32116078A>G	NCBI36
NG_007941.2:g.7015A>G
NG_008337.2:g.74053T>C
NG_007941.3:g.7018A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.940-84A>G MANE Select	ENSP00000496625.1:n.940-84A>G
ENST00000418967.6:c.940-84A>G	ENSP00000408860.2:n.940-84A>G
ENST00000435122.3:c.850-84A>G	ENSP00000415043.2:n.850-84A>G
ENST00000479074.5:n.998-84A>G
ENST00000479730.5:n.1056-84A>G
ENST00000483041.5:n.1109-84A>G
ENST00000486063.5:n.919-84A>G
NM_000500.7:c.940-84A>G	NP_000491.4:n.940-84A>G
NM_001128590.3:c.850-84A>G	NP_001122062.3:n.850-84A>G
XM_011514314.1:c.535-84A>G	XP_011512616.1:n.535-84A>G
NM_000500.9:c.940-84A>G MANE Select	NP_000491.4:n.940-84A>G
NM_001368143.1:c.535-84A>G	NP_001355072.1:n.535-84A>G
NM_001368144.1:c.535-84A>G	NP_001355073.1:n.535-84A>G
NM_001128590.4:c.850-84A>G	NP_001122062.3:n.850-84A>G
NM_001368143.2:c.535-84A>G	NP_001355072.1:n.535-84A>G
NM_001368144.2:c.535-84A>G	NP_001355073.1:n.535-84A>G