Canonical Allele Identifier: CA1619396326

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038402G= , CM000668.2:g.32038402G=	GRCh38
NC_000006.11:g.32006179G= , CM000668.1:g.32006179G=	GRCh37
NC_000006.10:g.32114158G=	NCBI36
NG_007941.2:g.5098G=
NG_007941.3:g.5098G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418967.6:c.-21G=	ENSP00000408860.2:n.-21G=
ENST00000466779.5:c.-21G=	ENSP00000417321.1:n.-21G=
ENST00000478281.5:c.-21G=	ENSP00000419572.1:n.-21G=
ENST00000479074.5:n.38G=
ENST00000479730.5:n.38G=
ENST00000480027.1:n.33G=
ENST00000483041.5:n.33G=
ENST00000486063.5:n.63G=
NM_000500.7:c.-21G=	NP_000491.4:n.-21G=
NM_001128590.3:c.-21G=	NP_001122062.3:n.-21G=
XM_011514314.1:c.-445G=	XP_011512616.1:n.-445G=
NM_001368143.1:c.-445G=	NP_001355072.1:n.-445G=
NM_001368144.1:c.-355G=	NP_001355073.1:n.-355G=