Canonical Allele Identifier: CA2678088874

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32039996-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039996C>G , CM000668.2:g.32039996C>G	GRCh38
NC_000006.11:g.32007773C>G , CM000668.1:g.32007773C>G	GRCh37
NC_000006.10:g.32115752C>G	NCBI36
NG_007941.2:g.6689C>G
NG_008337.2:g.74379G>C
NG_007941.3:g.6692C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.739-9C>G MANE Select	ENSP00000496625.1:n.739-9C>G
ENST00000418967.6:c.739-9C>G	ENSP00000408860.2:n.739-9C>G
ENST00000435122.3:c.649-9C>G	ENSP00000415043.2:n.649-9C>G
ENST00000479074.5:n.797-9C>G
ENST00000479730.5:n.855-9C>G
ENST00000483041.5:n.908-9C>G
ENST00000486063.5:n.918+161C>G
NM_000500.7:c.739-9C>G	NP_000491.4:n.739-9C>G
NM_001128590.3:c.649-9C>G	NP_001122062.3:n.649-9C>G
XM_011514314.1:c.334-9C>G	XP_011512616.1:n.334-9C>G
NM_000500.9:c.739-9C>G MANE Select	NP_000491.4:n.739-9C>G
NM_001368143.1:c.334-9C>G	NP_001355072.1:n.334-9C>G
NM_001368144.1:c.334-9C>G	NP_001355073.1:n.334-9C>G
NM_001128590.4:c.649-9C>G	NP_001122062.3:n.649-9C>G
NM_001368143.2:c.334-9C>G	NP_001355072.1:n.334-9C>G
NM_001368144.2:c.334-9C>G	NP_001355073.1:n.334-9C>G