Canonical Allele Identifier: CA363504204

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007405A>T (hg19) ; chr6:g.32039628A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039628A>T , CM000668.2:g.32039628A>T	GRCh38
NC_000006.11:g.32007405A>T , CM000668.1:g.32007405A>T	GRCh37
NC_000006.10:g.32115384A>T	NCBI36
NG_007941.2:g.6321A>T
NG_008337.2:g.74747T>A
NG_007941.3:g.6324A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.632A>T MANE Select	ENSP00000496625.1:p.Asp211Val
ENST00000418967.6:c.632A>T	ENSP00000408860.2:p.Asp211Val
ENST00000435122.3:c.542A>T	ENSP00000415043.2:p.Asp181Val
ENST00000462278.1:n.220A>T
ENST00000464325.5:n.553A>T
ENST00000466779.5:c.*324A>T	ENSP00000417321.1:n.*324A>T
ENST00000466879.5:n.683A>T
ENST00000469053.5:c.*324A>T	ENSP00000418104.1:n.*324A>T
ENST00000479074.5:n.690A>T
ENST00000479730.5:n.748A>T
ENST00000483041.5:n.801A>T
ENST00000486063.5:n.812A>T
NM_000500.7:c.632A>T	NP_000491.4:p.Asp211Val
NM_001128590.3:c.542A>T	NP_001122062.3:p.Asp181Val
XM_011514314.1:c.227A>T	XP_011512616.1:p.Asp76Val
NM_000500.9:c.632A>T MANE Select	NP_000491.4:p.Asp211Val
NM_001368143.1:c.227A>T	NP_001355072.1:p.Asp76Val
NM_001368144.1:c.227A>T	NP_001355073.1:p.Asp76Val
NM_001128590.4:c.542A>T	NP_001122062.3:p.Asp181Val
NM_001368143.2:c.227A>T	NP_001355072.1:p.Asp76Val
NM_001368144.2:c.227A>T	NP_001355073.1:p.Asp76Val