Canonical Allele Identifier: CA449818593

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007540A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039763A>T , CM000668.2:g.32039763A>T	GRCh38
NC_000006.11:g.32007540A>T , CM000668.1:g.32007540A>T	GRCh37
NC_000006.10:g.32115519A>T	NCBI36
NG_007941.2:g.6456A>T
NG_008337.2:g.74612T>A
NG_007941.3:g.6459A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.666A>T MANE Select	ENSP00000496625.1:p.Pro222=
ENST00000418967.6:c.666A>T	ENSP00000408860.2:p.Pro222=
ENST00000435122.3:c.576A>T	ENSP00000415043.2:p.Pro192=
ENST00000462278.1:n.355A>T
ENST00000466779.5:c.*358A>T	ENSP00000417321.1:n.*358A>T
ENST00000466879.5:n.717A>T
ENST00000479074.5:n.724A>T
ENST00000479730.5:n.782A>T
ENST00000483041.5:n.835A>T
ENST00000486063.5:n.846A>T
NM_000500.7:c.666A>T	NP_000491.4:p.Pro222=
NM_001128590.3:c.576A>T	NP_001122062.3:p.Pro192=
XM_011514314.1:c.261A>T	XP_011512616.1:p.Pro87=
NM_000500.9:c.666A>T MANE Select	NP_000491.4:p.Pro222=
NM_001368143.1:c.261A>T	NP_001355072.1:p.Pro87=
NM_001368144.1:c.261A>T	NP_001355073.1:p.Pro87=
NM_001128590.4:c.576A>T	NP_001122062.3:p.Pro192=
NM_001368143.2:c.261A>T	NP_001355072.1:p.Pro87=
NM_001368144.2:c.261A>T	NP_001355073.1:p.Pro87=