Canonical Allele Identifier: CA449818719

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007403G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039626G>C , CM000668.2:g.32039626G>C	GRCh38
NC_000006.11:g.32007403G>C , CM000668.1:g.32007403G>C	GRCh37
NC_000006.10:g.32115382G>C	NCBI36
NG_007941.2:g.6319G>C
NG_008337.2:g.74749C>G
NG_007941.3:g.6322G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.630G>C MANE Select	ENSP00000496625.1:p.Val210=
ENST00000418967.6:c.630G>C	ENSP00000408860.2:p.Val210=
ENST00000435122.3:c.540G>C	ENSP00000415043.2:p.Val180=
ENST00000462278.1:n.218G>C
ENST00000464325.5:n.551G>C
ENST00000466779.5:c.*322G>C	ENSP00000417321.1:n.*322G>C
ENST00000466879.5:n.681G>C
ENST00000469053.5:c.*322G>C	ENSP00000418104.1:n.*322G>C
ENST00000479074.5:n.688G>C
ENST00000479730.5:n.746G>C
ENST00000483041.5:n.799G>C
ENST00000486063.5:n.810G>C
NM_000500.7:c.630G>C	NP_000491.4:p.Val210=
NM_001128590.3:c.540G>C	NP_001122062.3:p.Val180=
XM_011514314.1:c.225G>C	XP_011512616.1:p.Val75=
NM_000500.9:c.630G>C MANE Select	NP_000491.4:p.Val210=
NM_001368143.1:c.225G>C	NP_001355072.1:p.Val75=
NM_001368144.1:c.225G>C	NP_001355073.1:p.Val75=
NM_001128590.4:c.540G>C	NP_001122062.3:p.Val180=
NM_001368143.2:c.225G>C	NP_001355072.1:p.Val75=
NM_001368144.2:c.225G>C	NP_001355073.1:p.Val75=