Canonical Allele Identifier: CA3732404

Gene: CYP21A2

Linked Data

• ClinVar Variation Id: 2634176
• ClinVar RCV Id: RCV003429045
• dbSNP Id: rs577450124
• ExAC: 6:32007133 C / A
• gnomAD v2: 6-32007133-C-A
• gnomAD v4: 6-32039356-C-A
• MyVariant Identifiers: chr6:g.32007133C>A (hg19) ; chr6:g.32039356C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039356C>A , CM000668.2:g.32039356C>A	GRCh38
NC_000006.11:g.32007133C>A , CM000668.1:g.32007133C>A	GRCh37
NC_000006.10:g.32115112C>A	NCBI36
NG_007941.2:g.6049C>A
NG_008337.2:g.75019G>T
NG_007941.3:g.6052C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.448C>A MANE Select	ENSP00000496625.1:p.Arg150Ser
ENST00000418967.6:c.448C>A	ENSP00000408860.2:p.Arg150Ser
ENST00000435122.3:c.358C>A	ENSP00000415043.2:p.Arg120Ser
ENST00000462278.1:n.36C>A
ENST00000464325.5:n.369C>A
ENST00000466779.5:c.*140C>A	ENSP00000417321.1:n.*140C>A
ENST00000466879.5:n.499C>A
ENST00000469053.5:c.*140C>A	ENSP00000418104.1:n.*140C>A
ENST00000471671.4:c.448C>A	ENSP00000418561.1:p.Arg150Ser
ENST00000478281.5:c.481C>A	ENSP00000419572.1:p.Arg161Ser
ENST00000479074.5:n.506C>A
ENST00000479730.5:n.603C>A
ENST00000483041.5:n.617C>A
ENST00000486063.5:n.628C>A
ENST00000488465.1:n.456C>A
NM_000500.7:c.448C>A	NP_000491.4:p.Arg150Ser
NM_001128590.3:c.358C>A	NP_001122062.3:p.Arg120Ser
XM_011514314.1:c.43C>A	XP_011512616.1:p.Arg15Ser
NM_000500.9:c.448C>A MANE Select	NP_000491.4:p.Arg150Ser
NM_001368143.1:c.43C>A	NP_001355072.1:p.Arg15Ser
NM_001368144.1:c.43C>A	NP_001355073.1:p.Arg15Ser
NM_001128590.4:c.358C>A	NP_001122062.3:p.Arg120Ser
NM_001368143.2:c.43C>A	NP_001355072.1:p.Arg15Ser
NM_001368144.2:c.43C>A	NP_001355073.1:p.Arg15Ser