Canonical Allele Identifier: CA363504063

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1306478015
• gnomAD v4: 6-32039615-A-G
• MyVariant Identifiers: chr6:g.32007392A>G (hg19) ; chr6:g.32039615A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039615A>G , CM000668.2:g.32039615A>G	GRCh38
NC_000006.11:g.32007392A>G , CM000668.1:g.32007392A>G	GRCh37
NC_000006.10:g.32115371A>G	NCBI36
NG_007941.2:g.6308A>G
NG_008337.2:g.74760T>C
NG_007941.3:g.6311A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.619A>G MANE Select	ENSP00000496625.1:p.Ile207Val
ENST00000418967.6:c.619A>G	ENSP00000408860.2:p.Ile207Val
ENST00000435122.3:c.529A>G	ENSP00000415043.2:p.Ile177Val
ENST00000462278.1:n.207A>G
ENST00000464325.5:n.540A>G
ENST00000466779.5:c.*311A>G	ENSP00000417321.1:n.*311A>G
ENST00000466879.5:n.670A>G
ENST00000469053.5:c.*311A>G	ENSP00000418104.1:n.*311A>G
ENST00000479074.5:n.677A>G
ENST00000479730.5:n.735A>G
ENST00000483041.5:n.788A>G
ENST00000486063.5:n.799A>G
NM_000500.7:c.619A>G	NP_000491.4:p.Ile207Val
NM_001128590.3:c.529A>G	NP_001122062.3:p.Ile177Val
XM_011514314.1:c.214A>G	XP_011512616.1:p.Ile72Val
NM_000500.9:c.619A>G MANE Select	NP_000491.4:p.Ile207Val
NM_001368143.1:c.214A>G	NP_001355072.1:p.Ile72Val
NM_001368144.1:c.214A>G	NP_001355073.1:p.Ile72Val
NM_001128590.4:c.529A>G	NP_001122062.3:p.Ile177Val
NM_001368143.2:c.214A>G	NP_001355072.1:p.Ile72Val
NM_001368144.2:c.214A>G	NP_001355073.1:p.Ile72Val