Canonical Allele Identifier: CA363512665

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008852T>G (hg19) ; chr6:g.32041075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041075T>G , CM000668.2:g.32041075T>G	GRCh38
NC_000006.11:g.32008852T>G , CM000668.1:g.32008852T>G	GRCh37
NC_000006.10:g.32116831T>G	NCBI36
NG_007941.2:g.7768T>G
NG_008337.2:g.73300A>C
NG_007941.3:g.7771T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1429T>G MANE Select	ENSP00000496625.1:p.Phe477Val
ENST00000418967.6:c.1429T>G	ENSP00000408860.2:p.Phe477Val
ENST00000435122.3:c.1339T>G	ENSP00000415043.2:p.Phe447Val
ENST00000479074.5:n.1570T>G
ENST00000479730.5:n.1545T>G
ENST00000483041.5:n.1598T>G
ENST00000486063.5:n.1408T>G
NM_000500.7:c.1429T>G	NP_000491.4:p.Phe477Val
NM_001128590.3:c.1339T>G	NP_001122062.3:p.Phe447Val
XM_011514314.1:c.1024T>G	XP_011512616.1:p.Phe342Val
NM_000500.9:c.1429T>G MANE Select	NP_000491.4:p.Phe477Val
NM_001368143.1:c.1024T>G	NP_001355072.1:p.Phe342Val
NM_001368144.1:c.1024T>G	NP_001355073.1:p.Phe342Val
NM_001128590.4:c.1339T>G	NP_001122062.3:p.Phe447Val
NM_001368143.2:c.1024T>G	NP_001355072.1:p.Phe342Val
NM_001368144.2:c.1024T>G	NP_001355073.1:p.Phe342Val