Canonical Allele Identifier: CA363505395

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007596A>G (hg19) ; chr6:g.32039819A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039819A>G , CM000668.2:g.32039819A>G	GRCh38
NC_000006.11:g.32007596A>G , CM000668.1:g.32007596A>G	GRCh37
NC_000006.10:g.32115575A>G	NCBI36
NG_007941.2:g.6512A>G
NG_008337.2:g.74556T>C
NG_007941.3:g.6515A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.722A>G MANE Select	ENSP00000496625.1:p.Gln241Arg
ENST00000418967.6:c.722A>G	ENSP00000408860.2:p.Gln241Arg
ENST00000435122.3:c.632A>G	ENSP00000415043.2:p.Gln211Arg
ENST00000462278.1:n.411A>G
ENST00000466779.5:c.*414A>G	ENSP00000417321.1:n.*414A>G
ENST00000466879.5:n.773A>G
ENST00000479074.5:n.780A>G
ENST00000479730.5:n.838A>G
ENST00000483041.5:n.891A>G
ENST00000486063.5:n.902A>G
NM_000500.7:c.722A>G	NP_000491.4:p.Gln241Arg
NM_001128590.3:c.632A>G	NP_001122062.3:p.Gln211Arg
XM_011514314.1:c.317A>G	XP_011512616.1:p.Gln106Arg
NM_000500.9:c.722A>G MANE Select	NP_000491.4:p.Gln241Arg
NM_001368143.1:c.317A>G	NP_001355072.1:p.Gln106Arg
NM_001368144.1:c.317A>G	NP_001355073.1:p.Gln106Arg
NM_001128590.4:c.632A>G	NP_001122062.3:p.Gln211Arg
NM_001368143.2:c.317A>G	NP_001355072.1:p.Gln106Arg
NM_001368144.2:c.317A>G	NP_001355073.1:p.Gln106Arg