Canonical Allele Identifier: CA363503154

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007218T>C (hg19) ; chr6:g.32039441T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039441T>C , CM000668.2:g.32039441T>C	GRCh38
NC_000006.11:g.32007218T>C , CM000668.1:g.32007218T>C	GRCh37
NC_000006.10:g.32115197T>C	NCBI36
NG_007941.2:g.6134T>C
NG_008337.2:g.74934A>G
NG_007941.3:g.6137T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.533T>C MANE Select	ENSP00000496625.1:p.Phe178Ser
ENST00000418967.6:c.533T>C	ENSP00000408860.2:p.Phe178Ser
ENST00000435122.3:c.443T>C	ENSP00000415043.2:p.Phe148Ser
ENST00000462278.1:n.121T>C
ENST00000464325.5:n.454T>C
ENST00000466779.5:c.*225T>C	ENSP00000417321.1:n.*225T>C
ENST00000466879.5:n.584T>C
ENST00000469053.5:c.*225T>C	ENSP00000418104.1:n.*225T>C
ENST00000471671.4:c.533T>C	ENSP00000418561.1:p.Phe178Ser
ENST00000479074.5:n.591T>C
ENST00000479730.5:n.688T>C
ENST00000483041.5:n.702T>C
ENST00000486063.5:n.713T>C
ENST00000488465.1:n.541T>C
NM_000500.7:c.533T>C	NP_000491.4:p.Phe178Ser
NM_001128590.3:c.443T>C	NP_001122062.3:p.Phe148Ser
XM_011514314.1:c.128T>C	XP_011512616.1:p.Phe43Ser
NM_000500.9:c.533T>C MANE Select	NP_000491.4:p.Phe178Ser
NM_001368143.1:c.128T>C	NP_001355072.1:p.Phe43Ser
NM_001368144.1:c.128T>C	NP_001355073.1:p.Phe43Ser
NM_001128590.4:c.443T>C	NP_001122062.3:p.Phe148Ser
NM_001368143.2:c.128T>C	NP_001355072.1:p.Phe43Ser
NM_001368144.2:c.128T>C	NP_001355073.1:p.Phe43Ser