Canonical Allele Identifier: CA363506117

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1213221369
• gnomAD v2: 6-32007819-A-G
• gnomAD v4: 6-32040042-A-G
• MyVariant Identifiers: chr6:g.32007819A>G (hg19) ; chr6:g.32040042A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040042A>G , CM000668.2:g.32040042A>G	GRCh38
NC_000006.11:g.32007819A>G , CM000668.1:g.32007819A>G	GRCh37
NC_000006.10:g.32115798A>G	NCBI36
NG_007941.2:g.6735A>G
NG_008337.2:g.74333T>C
NG_007941.3:g.6738A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.776A>G MANE Select	ENSP00000496625.1:p.Asp259Gly
ENST00000418967.6:c.776A>G	ENSP00000408860.2:p.Asp259Gly
ENST00000435122.3:c.686A>G	ENSP00000415043.2:p.Asp229Gly
ENST00000479074.5:n.834A>G
ENST00000479730.5:n.892A>G
ENST00000483041.5:n.945A>G
ENST00000486063.5:n.918+207A>G
NM_000500.7:c.776A>G	NP_000491.4:p.Asp259Gly
NM_001128590.3:c.686A>G	NP_001122062.3:p.Asp229Gly
XM_011514314.1:c.371A>G	XP_011512616.1:p.Asp124Gly
NM_000500.9:c.776A>G MANE Select	NP_000491.4:p.Asp259Gly
NM_001368143.1:c.371A>G	NP_001355072.1:p.Asp124Gly
NM_001368144.1:c.371A>G	NP_001355073.1:p.Asp124Gly
NM_001128590.4:c.686A>G	NP_001122062.3:p.Asp229Gly
NM_001368143.2:c.371A>G	NP_001355072.1:p.Asp124Gly
NM_001368144.2:c.371A>G	NP_001355073.1:p.Asp124Gly