Canonical Allele Identifier: CA823930557

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1401769980
• gnomAD v3: 6-32039341-A-G
• gnomAD v4: 6-32039341-A-G
• MyVariant Identifiers: chr6:g.32007118A>G (hg19) ; chr6:g.32039341A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039341A>G , CM000668.2:g.32039341A>G	GRCh38
NC_000006.11:g.32007118A>G , CM000668.1:g.32007118A>G	GRCh37
NC_000006.10:g.32115097A>G	NCBI36
NG_007941.2:g.6034A>G
NG_008337.2:g.75034T>C
NG_007941.3:g.6037A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.448-15A>G MANE Select	ENSP00000496625.1:n.448-15A>G
ENST00000418967.6:c.448-15A>G	ENSP00000408860.2:n.448-15A>G
ENST00000435122.3:c.358-15A>G	ENSP00000415043.2:n.358-15A>G
ENST00000462278.1:n.36-15A>G
ENST00000464325.5:n.369-15A>G
ENST00000466779.5:c.*140-15A>G	ENSP00000417321.1:n.*140-15A>G
ENST00000466879.5:n.499-15A>G
ENST00000469053.5:c.*140-15A>G	ENSP00000418104.1:n.*140-15A>G
ENST00000471671.4:c.448-15A>G	ENSP00000418561.1:n.448-15A>G
ENST00000478281.5:c.481-15A>G	ENSP00000419572.1:n.481-15A>G
ENST00000479074.5:n.506-15A>G
ENST00000479730.5:n.603-15A>G
ENST00000483041.5:n.617-15A>G
ENST00000486063.5:n.628-15A>G
ENST00000488465.1:n.456-15A>G
NM_000500.7:c.448-15A>G	NP_000491.4:n.448-15A>G
NM_001128590.3:c.358-15A>G	NP_001122062.3:n.358-15A>G
XM_011514314.1:c.43-15A>G	XP_011512616.1:n.43-15A>G
NM_000500.9:c.448-15A>G MANE Select	NP_000491.4:n.448-15A>G
NM_001368143.1:c.43-15A>G	NP_001355072.1:n.43-15A>G
NM_001368144.1:c.43-15A>G	NP_001355073.1:n.43-15A>G
NM_001128590.4:c.358-15A>G	NP_001122062.3:n.358-15A>G
NM_001368143.2:c.43-15A>G	NP_001355072.1:n.43-15A>G
NM_001368144.2:c.43-15A>G	NP_001355073.1:n.43-15A>G