Canonical Allele Identifier: CA363500231

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32038813-T-C
• MyVariant Identifiers: chr6:g.32006590T>C (hg19) ; chr6:g.32038813T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038813T>C , CM000668.2:g.32038813T>C	GRCh38
NC_000006.11:g.32006590T>C , CM000668.1:g.32006590T>C	GRCh37
NC_000006.10:g.32114569T>C	NCBI36
NG_007941.2:g.5506T>C
NG_007941.3:g.5509T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.292+2T>C MANE Select	ENSP00000496625.1:n.292+2T>C
ENST00000418967.6:c.292+2T>C	ENSP00000408860.2:n.292+2T>C
ENST00000435122.3:c.202+189T>C	ENSP00000415043.2:n.202+189T>C
ENST00000464325.5:n.229+2T>C
ENST00000466779.5:c.292+2T>C	ENSP00000417321.1:n.292+2T>C
ENST00000466879.5:n.63T>C
ENST00000469053.5:c.202+189T>C	ENSP00000418104.1:n.202+189T>C
ENST00000471671.4:c.292+2T>C	ENSP00000418561.1:n.292+2T>C
ENST00000478281.5:c.292+2T>C	ENSP00000419572.1:n.292+2T>C
ENST00000479074.5:n.350+2T>C
ENST00000479730.5:n.447+2T>C
ENST00000480027.1:n.347T>C
ENST00000483041.5:n.442+2T>C
ENST00000486063.5:n.472+2T>C
ENST00000488465.1:n.300+2T>C
NM_000500.7:c.292+2T>C	NP_000491.4:n.292+2T>C
NM_001128590.3:c.202+189T>C	NP_001122062.3:n.202+189T>C
XM_011514314.1:c.-133+2T>C	XP_011512616.1:n.-133+2T>C
NM_000500.9:c.292+2T>C MANE Select	NP_000491.4:n.292+2T>C
NM_001368143.1:c.-133+2T>C	NP_001355072.1:n.-133+2T>C
NM_001368144.1:c.-133+189T>C	NP_001355073.1:n.-133+189T>C
NM_001128590.4:c.202+189T>C	NP_001122062.3:n.202+189T>C
NM_001368143.2:c.-133+2T>C	NP_001355072.1:n.-133+2T>C
NM_001368144.2:c.-133+189T>C	NP_001355073.1:n.-133+189T>C