Canonical Allele Identifier: CA449729681

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007871G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040094G>A , CM000668.2:g.32040094G>A	GRCh38
NC_000006.11:g.32007871G>A , CM000668.1:g.32007871G>A	GRCh37
NC_000006.10:g.32115850G>A	NCBI36
NG_007941.2:g.6787G>A
NG_008337.2:g.74281C>T
NG_007941.3:g.6790G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.828G>A MANE Select	ENSP00000496625.1:p.Gln276=
ENST00000418967.6:c.828G>A	ENSP00000408860.2:p.Gln276=
ENST00000435122.3:c.738G>A	ENSP00000415043.2:p.Gln246=
ENST00000479074.5:n.886G>A
ENST00000479730.5:n.944G>A
ENST00000483041.5:n.997G>A
ENST00000486063.5:n.918+259G>A
NM_000500.7:c.828G>A	NP_000491.4:p.Gln276=
NM_001128590.3:c.738G>A	NP_001122062.3:p.Gln246=
XM_011514314.1:c.423G>A	XP_011512616.1:p.Gln141=
NM_000500.9:c.828G>A MANE Select	NP_000491.4:p.Gln276=
NM_001368143.1:c.423G>A	NP_001355072.1:p.Gln141=
NM_001368144.1:c.423G>A	NP_001355073.1:p.Gln141=
NM_001128590.4:c.738G>A	NP_001122062.3:p.Gln246=
NM_001368143.2:c.423G>A	NP_001355072.1:p.Gln141=
NM_001368144.2:c.423G>A	NP_001355073.1:p.Gln141=