Canonical Allele Identifier: CA363499353

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32006365T>C (hg19) ; chr6:g.32038588T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038588T>C , CM000668.2:g.32038588T>C	GRCh38
NC_000006.11:g.32006365T>C , CM000668.1:g.32006365T>C	GRCh37
NC_000006.10:g.32114344T>C	NCBI36
NG_007941.2:g.5281T>C
NG_007941.3:g.5284T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.166T>C MANE Select	ENSP00000496625.1:p.Phe56Leu
ENST00000418967.6:c.166T>C	ENSP00000408860.2:p.Phe56Leu
ENST00000435122.3:c.166T>C	ENSP00000415043.2:p.Phe56Leu
ENST00000464325.5:n.6T>C
ENST00000466779.5:c.166T>C	ENSP00000417321.1:p.Phe56Leu
ENST00000469053.5:c.166T>C	ENSP00000418104.1:p.Phe56Leu
ENST00000471671.4:c.166T>C	ENSP00000418561.1:p.Phe56Leu
ENST00000478281.5:c.166T>C	ENSP00000419572.1:p.Phe56Leu
ENST00000479074.5:n.224T>C
ENST00000479730.5:n.224T>C
ENST00000480027.1:n.219T>C
ENST00000483041.5:n.219T>C
ENST00000486063.5:n.249T>C
ENST00000488465.1:n.174T>C
NM_000500.7:c.166T>C	NP_000491.4:p.Phe56Leu
NM_001128590.3:c.166T>C	NP_001122062.3:p.Phe56Leu
XM_011514314.1:c.-259T>C	XP_011512616.1:n.-259T>C
NM_000500.9:c.166T>C MANE Select	NP_000491.4:p.Phe56Leu
NM_001368143.1:c.-259T>C	NP_001355072.1:n.-259T>C
NM_001368144.1:c.-169T>C	NP_001355073.1:n.-169T>C
NM_001128590.4:c.166T>C	NP_001122062.3:p.Phe56Leu
NM_001368143.2:c.-259T>C	NP_001355072.1:n.-259T>C
NM_001368144.2:c.-169T>C	NP_001355073.1:n.-169T>C