Canonical Allele Identifier: CA363507424

Gene: CYP21A2

Linked Data

• ClinVar Variation Id: 3079400
• ClinVar RCV Id: RCV004367794
• dbSNP Id: rs1776190245
• MyVariant Identifiers: chr6:g.32007954C>G (hg19) ; chr6:g.32040177C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040177C>G , CM000668.2:g.32040177C>G	GRCh38
NC_000006.11:g.32007954C>G , CM000668.1:g.32007954C>G	GRCh37
NC_000006.10:g.32115933C>G	NCBI36
NG_007941.2:g.6870C>G
NG_008337.2:g.74198G>C
NG_007941.3:g.6873C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.911C>G MANE Select	ENSP00000496625.1:p.Ala304Gly
ENST00000418967.6:c.911C>G	ENSP00000408860.2:p.Ala304Gly
ENST00000435122.3:c.821C>G	ENSP00000415043.2:p.Ala274Gly
ENST00000479074.5:n.969C>G
ENST00000479730.5:n.1027C>G
ENST00000483041.5:n.1080C>G
ENST00000486063.5:n.919-229C>G
NM_000500.7:c.911C>G	NP_000491.4:p.Ala304Gly
NM_001128590.3:c.821C>G	NP_001122062.3:p.Ala274Gly
XM_011514314.1:c.506C>G	XP_011512616.1:p.Ala169Gly
NM_000500.9:c.911C>G MANE Select	NP_000491.4:p.Ala304Gly
NM_001368143.1:c.506C>G	NP_001355072.1:p.Ala169Gly
NM_001368144.1:c.506C>G	NP_001355073.1:p.Ala169Gly
NM_001128590.4:c.821C>G	NP_001122062.3:p.Ala274Gly
NM_001368143.2:c.506C>G	NP_001355072.1:p.Ala169Gly
NM_001368144.2:c.506C>G	NP_001355073.1:p.Ala169Gly