Canonical Allele Identifier: CA136893296

Gene: CYP21A2

Linked Data

• dbSNP Id: rs879281716
• MyVariant Identifiers: chr6:g.32006295T>C (hg19) ; chr6:g.32038518T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038518T>C , CM000668.2:g.32038518T>C	GRCh38
NC_000006.11:g.32006295T>C , CM000668.1:g.32006295T>C	GRCh37
NC_000006.10:g.32114274T>C	NCBI36
NG_007941.2:g.5211T>C
NG_007941.3:g.5214T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.96T>C MANE Select	ENSP00000496625.1:p.Pro32=
ENST00000418967.6:c.96T>C	ENSP00000408860.2:p.Pro32=
ENST00000435122.3:c.96T>C	ENSP00000415043.2:p.Pro32=
ENST00000466779.5:c.96T>C	ENSP00000417321.1:p.Pro32=
ENST00000469053.5:c.96T>C	ENSP00000418104.1:p.Pro32=
ENST00000471671.4:c.96T>C	ENSP00000418561.1:p.Pro32=
ENST00000478281.5:c.96T>C	ENSP00000419572.1:p.Pro32=
ENST00000479074.5:n.154T>C
ENST00000479730.5:n.154T>C
ENST00000480027.1:n.149T>C
ENST00000483041.5:n.149T>C
ENST00000486063.5:n.179T>C
ENST00000488465.1:n.104T>C
NM_000500.7:c.96T>C	NP_000491.4:p.Pro32=
NM_001128590.3:c.96T>C	NP_001122062.3:p.Pro32=
XM_011514314.1:c.-329T>C	XP_011512616.1:n.-329T>C
NM_000500.9:c.96T>C MANE Select	NP_000491.4:p.Pro32=
NM_001368143.1:c.-329T>C	NP_001355072.1:n.-329T>C
NM_001368144.1:c.-239T>C	NP_001355073.1:n.-239T>C
NM_001128590.4:c.96T>C	NP_001122062.3:p.Pro32=
NM_001368143.2:c.-329T>C	NP_001355072.1:n.-329T>C
NM_001368144.2:c.-239T>C	NP_001355073.1:n.-239T>C