Canonical Allele Identifier: CA566693902

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1251687806
• gnomAD v2: 6-32007455-T-A
• gnomAD v4: 6-32039678-T-A
• MyVariant Identifiers: chr6:g.32007455T>A (hg19) ; chr6:g.32039678T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039678T>A , CM000668.2:g.32039678T>A	GRCh38
NC_000006.11:g.32007455T>A , CM000668.1:g.32007455T>A	GRCh37
NC_000006.10:g.32115434T>A	NCBI36
NG_007941.2:g.6371T>A
NG_008337.2:g.74697A>T
NG_007941.3:g.6374T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.651+31T>A MANE Select	ENSP00000496625.1:n.651+31T>A
ENST00000418967.6:c.651+31T>A	ENSP00000408860.2:n.651+31T>A
ENST00000435122.3:c.561+31T>A	ENSP00000415043.2:n.561+31T>A
ENST00000462278.1:n.270T>A
ENST00000464325.5:n.572+31T>A
ENST00000466779.5:c.*343+31T>A	ENSP00000417321.1:n.*343+31T>A
ENST00000466879.5:n.702+31T>A
ENST00000479074.5:n.709+31T>A
ENST00000479730.5:n.767+31T>A
ENST00000483041.5:n.820+31T>A
ENST00000486063.5:n.831+31T>A
NM_000500.7:c.651+31T>A	NP_000491.4:n.651+31T>A
NM_001128590.3:c.561+31T>A	NP_001122062.3:n.561+31T>A
XM_011514314.1:c.246+31T>A	XP_011512616.1:n.246+31T>A
NM_000500.9:c.651+31T>A MANE Select	NP_000491.4:n.651+31T>A
NM_001368143.1:c.246+31T>A	NP_001355072.1:n.246+31T>A
NM_001368144.1:c.246+31T>A	NP_001355073.1:n.246+31T>A
NM_001128590.4:c.561+31T>A	NP_001122062.3:n.561+31T>A
NM_001368143.2:c.246+31T>A	NP_001355072.1:n.246+31T>A
NM_001368144.2:c.246+31T>A	NP_001355073.1:n.246+31T>A