Canonical Allele Identifier: CA449818814

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008311G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040534G>A , CM000668.2:g.32040534G>A	GRCh38
NC_000006.11:g.32008311G>A , CM000668.1:g.32008311G>A	GRCh37
NC_000006.10:g.32116290G>A	NCBI36
NG_007941.2:g.7227G>A
NG_008337.2:g.73841C>T
NG_007941.3:g.7230G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1068G>A MANE Select	ENSP00000496625.1:p.Leu356=
ENST00000418967.6:c.1068G>A	ENSP00000408860.2:p.Leu356=
ENST00000435122.3:c.978G>A	ENSP00000415043.2:p.Leu326=
ENST00000479074.5:n.1126G>A
ENST00000479730.5:n.1184G>A
ENST00000483041.5:n.1237G>A
ENST00000486063.5:n.1047G>A
NM_000500.7:c.1068G>A	NP_000491.4:p.Leu356=
NM_001128590.3:c.978G>A	NP_001122062.3:p.Leu326=
XM_011514314.1:c.663G>A	XP_011512616.1:p.Leu221=
NM_000500.9:c.1068G>A MANE Select	NP_000491.4:p.Leu356=
NM_001368143.1:c.663G>A	NP_001355072.1:p.Leu221=
NM_001368144.1:c.663G>A	NP_001355073.1:p.Leu221=
NM_001128590.4:c.978G>A	NP_001122062.3:p.Leu326=
NM_001368143.2:c.663G>A	NP_001355072.1:p.Leu221=
NM_001368144.2:c.663G>A	NP_001355073.1:p.Leu221=