Canonical Allele Identifier: CA2678088245

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32038391-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038391T>C , CM000668.2:g.32038391T>C	GRCh38
NC_000006.11:g.32006168T>C , CM000668.1:g.32006168T>C	GRCh37
NC_000006.10:g.32114147T>C	NCBI36
NG_007941.2:g.5087T>C
NG_007941.3:g.5087T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418967.6:c.-32T>C	ENSP00000408860.2:n.-32T>C
ENST00000466779.5:c.-32T>C	ENSP00000417321.1:n.-32T>C
ENST00000478281.5:c.-32T>C	ENSP00000419572.1:n.-32T>C
ENST00000479074.5:n.27T>C
ENST00000479730.5:n.27T>C
ENST00000480027.1:n.22T>C
ENST00000483041.5:n.22T>C
ENST00000486063.5:n.52T>C
NM_000500.7:c.-32T>C	NP_000491.4:n.-32T>C
NM_001128590.3:c.-32T>C	NP_001122062.3:n.-32T>C
XM_011514314.1:c.-456T>C	XP_011512616.1:n.-456T>C
NM_001368143.1:c.-456T>C	NP_001355072.1:n.-456T>C
NM_001368144.1:c.-366T>C	NP_001355073.1:n.-366T>C