Canonical Allele Identifier: CA363498819

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32006273T>G (hg19) ; chr6:g.32038496T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038496T>G , CM000668.2:g.32038496T>G	GRCh38
NC_000006.11:g.32006273T>G , CM000668.1:g.32006273T>G	GRCh37
NC_000006.10:g.32114252T>G	NCBI36
NG_007941.2:g.5189T>G
NG_007941.3:g.5192T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.74T>G MANE Select	ENSP00000496625.1:p.Leu25Arg
ENST00000418967.6:c.74T>G	ENSP00000408860.2:p.Leu25Arg
ENST00000435122.3:c.74T>G	ENSP00000415043.2:p.Leu25Arg
ENST00000466779.5:c.74T>G	ENSP00000417321.1:p.Leu25Arg
ENST00000469053.5:c.74T>G	ENSP00000418104.1:p.Leu25Arg
ENST00000471671.4:c.74T>G	ENSP00000418561.1:p.Leu25Arg
ENST00000478281.5:c.74T>G	ENSP00000419572.1:p.Leu25Arg
ENST00000479074.5:n.132T>G
ENST00000479730.5:n.132T>G
ENST00000480027.1:n.127T>G
ENST00000483041.5:n.127T>G
ENST00000486063.5:n.157T>G
ENST00000488465.1:n.82T>G
NM_000500.7:c.74T>G	NP_000491.4:p.Leu25Arg
NM_001128590.3:c.74T>G	NP_001122062.3:p.Leu25Arg
XM_011514314.1:c.-351T>G	XP_011512616.1:n.-351T>G
NM_000500.9:c.74T>G MANE Select	NP_000491.4:p.Leu25Arg
NM_001368143.1:c.-351T>G	NP_001355072.1:n.-351T>G
NM_001368144.1:c.-261T>G	NP_001355073.1:n.-261T>G
NM_001128590.4:c.74T>G	NP_001122062.3:p.Leu25Arg
NM_001368143.2:c.-351T>G	NP_001355072.1:n.-351T>G
NM_001368144.2:c.-261T>G	NP_001355073.1:n.-261T>G