Canonical Allele Identifier: CA3732269

Gene: CYP21A2

Linked Data

• ClinVar Variation Id: 434880
• ClinVar RCV Id: RCV000503594
• dbSNP Id: rs72552744
• ExAC: 6:32006268 G / T
• gnomAD v2: 6-32006268-G-T
• gnomAD v3: 6-32038491-G-T
• gnomAD v4: 6-32038491-G-T
• MyVariant Identifiers: chr6:g.32006268G>T (hg19) ; chr6:g.32038491G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038491G>T , CM000668.2:g.32038491G>T	GRCh38
NC_000006.11:g.32006268G>T , CM000668.1:g.32006268G>T	GRCh37
NC_000006.10:g.32114247G>T	NCBI36
NG_007941.2:g.5184G>T
NG_007941.3:g.5187G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.69G>T MANE Select	ENSP00000496625.1:p.Trp23Cys
ENST00000418967.6:c.69G>T	ENSP00000408860.2:p.Trp23Cys
ENST00000435122.3:c.69G>T	ENSP00000415043.2:p.Trp23Cys
ENST00000466779.5:c.69G>T	ENSP00000417321.1:p.Trp23Cys
ENST00000469053.5:c.69G>T	ENSP00000418104.1:p.Trp23Cys
ENST00000471671.4:c.69G>T	ENSP00000418561.1:p.Trp23Cys
ENST00000478281.5:c.69G>T	ENSP00000419572.1:p.Trp23Cys
ENST00000479074.5:n.127G>T
ENST00000479730.5:n.127G>T
ENST00000480027.1:n.122G>T
ENST00000483041.5:n.122G>T
ENST00000486063.5:n.152G>T
ENST00000488465.1:n.77G>T
NM_000500.7:c.69G>T	NP_000491.4:p.Trp23Cys
NM_001128590.3:c.69G>T	NP_001122062.3:p.Trp23Cys
XM_011514314.1:c.-356G>T	XP_011512616.1:n.-356G>T
NM_000500.9:c.69G>T MANE Select	NP_000491.4:p.Trp23Cys
NM_001368143.1:c.-356G>T	NP_001355072.1:n.-356G>T
NM_001368144.1:c.-266G>T	NP_001355073.1:n.-266G>T
NM_001128590.4:c.69G>T	NP_001122062.3:p.Trp23Cys
NM_001368143.2:c.-356G>T	NP_001355072.1:n.-356G>T
NM_001368144.2:c.-266G>T	NP_001355073.1:n.-266G>T