Canonical Allele Identifier: CA3732472

Gene: CYP21A2

Linked Data

• dbSNP Id: rs763485273
• ExAC: 6:32007475 T / G
• gnomAD v2: 6-32007475-T-G
• gnomAD v4: 6-32039698-T-G
• MyVariant Identifiers: chr6:g.32007475T>G (hg19) ; chr6:g.32039698T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039698T>G , CM000668.2:g.32039698T>G	GRCh38
NC_000006.11:g.32007475T>G , CM000668.1:g.32007475T>G	GRCh37
NC_000006.10:g.32115454T>G	NCBI36
NG_007941.2:g.6391T>G
NG_008337.2:g.74677A>C
NG_007941.3:g.6394T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.652-51T>G MANE Select	ENSP00000496625.1:n.652-51T>G
ENST00000418967.6:c.652-51T>G	ENSP00000408860.2:n.652-51T>G
ENST00000435122.3:c.562-51T>G	ENSP00000415043.2:n.562-51T>G
ENST00000462278.1:n.290T>G
ENST00000464325.5:n.573-51T>G
ENST00000466779.5:c.*344-51T>G	ENSP00000417321.1:n.*344-51T>G
ENST00000466879.5:n.703-51T>G
ENST00000479074.5:n.710-51T>G
ENST00000479730.5:n.768-51T>G
ENST00000483041.5:n.821-51T>G
ENST00000486063.5:n.832-51T>G
NM_000500.7:c.652-51T>G	NP_000491.4:n.652-51T>G
NM_001128590.3:c.562-51T>G	NP_001122062.3:n.562-51T>G
XM_011514314.1:c.247-51T>G	XP_011512616.1:n.247-51T>G
NM_000500.9:c.652-51T>G MANE Select	NP_000491.4:n.652-51T>G
NM_001368143.1:c.247-51T>G	NP_001355072.1:n.247-51T>G
NM_001368144.1:c.247-51T>G	NP_001355073.1:n.247-51T>G
NM_001128590.4:c.562-51T>G	NP_001122062.3:n.562-51T>G
NM_001368143.2:c.247-51T>G	NP_001355072.1:n.247-51T>G
NM_001368144.2:c.247-51T>G	NP_001355073.1:n.247-51T>G