Canonical Allele Identifier: CA363504132

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007398A>G (hg19) ; chr6:g.32039621A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039621A>G , CM000668.2:g.32039621A>G	GRCh38
NC_000006.11:g.32007398A>G , CM000668.1:g.32007398A>G	GRCh37
NC_000006.10:g.32115377A>G	NCBI36
NG_007941.2:g.6314A>G
NG_008337.2:g.74754T>C
NG_007941.3:g.6317A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.625A>G MANE Select	ENSP00000496625.1:p.Ile209Val
ENST00000418967.6:c.625A>G	ENSP00000408860.2:p.Ile209Val
ENST00000435122.3:c.535A>G	ENSP00000415043.2:p.Ile179Val
ENST00000462278.1:n.213A>G
ENST00000464325.5:n.546A>G
ENST00000466779.5:c.*317A>G	ENSP00000417321.1:n.*317A>G
ENST00000466879.5:n.676A>G
ENST00000469053.5:c.*317A>G	ENSP00000418104.1:n.*317A>G
ENST00000479074.5:n.683A>G
ENST00000479730.5:n.741A>G
ENST00000483041.5:n.794A>G
ENST00000486063.5:n.805A>G
NM_000500.7:c.625A>G	NP_000491.4:p.Ile209Val
NM_001128590.3:c.535A>G	NP_001122062.3:p.Ile179Val
XM_011514314.1:c.220A>G	XP_011512616.1:p.Ile74Val
NM_000500.9:c.625A>G MANE Select	NP_000491.4:p.Ile209Val
NM_001368143.1:c.220A>G	NP_001355072.1:p.Ile74Val
NM_001368144.1:c.220A>G	NP_001355073.1:p.Ile74Val
NM_001128590.4:c.535A>G	NP_001122062.3:p.Ile179Val
NM_001368143.2:c.220A>G	NP_001355072.1:p.Ile74Val
NM_001368144.2:c.220A>G	NP_001355073.1:p.Ile74Val