Canonical Allele Identifier: CA1619396312

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1775973887
• gnomAD v4: 6-32038364-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038364G>A , CM000668.2:g.32038364G>A	GRCh38
NC_000006.11:g.32006141G>A , CM000668.1:g.32006141G>A	GRCh37
NC_000006.10:g.32114120G>A	NCBI36
NG_007941.2:g.5060G>A
NG_007941.3:g.5060G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418967.6:c.-59G>A	ENSP00000408860.2:n.-59G>A
ENST00000466779.5:c.-59G>A	ENSP00000417321.1:n.-59G>A
ENST00000486063.5:n.25G>A
NM_000500.7:c.-59G>A	NP_000491.4:n.-59G>A
NM_001128590.3:c.-59G>A	NP_001122062.3:n.-59G>A
NM_001368143.1:c.-483G>A	NP_001355072.1:n.-483G>A
NM_001368144.1:c.-393G>A	NP_001355073.1:n.-393G>A