Canonical Allele Identifier: CA363511195

Gene: CYP21A2

Linked Data

• dbSNP Id: rs2151875530
• gnomAD v4: 6-32040583-A-G
• MyVariant Identifiers: chr6:g.32008360A>G (hg19) ; chr6:g.32040583A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040583A>G , CM000668.2:g.32040583A>G	GRCh38
NC_000006.11:g.32008360A>G , CM000668.1:g.32008360A>G	GRCh37
NC_000006.10:g.32116339A>G	NCBI36
NG_007941.2:g.7276A>G
NG_008337.2:g.73792T>C
NG_007941.3:g.7279A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1117A>G MANE Select	ENSP00000496625.1:p.Ser373Gly
ENST00000418967.6:c.1117A>G	ENSP00000408860.2:p.Ser373Gly
ENST00000435122.3:c.1027A>G	ENSP00000415043.2:p.Ser343Gly
ENST00000479074.5:n.1175A>G
ENST00000479730.5:n.1233A>G
ENST00000483041.5:n.1286A>G
ENST00000486063.5:n.1096A>G
NM_000500.7:c.1117A>G	NP_000491.4:p.Ser373Gly
NM_001128590.3:c.1027A>G	NP_001122062.3:p.Ser343Gly
XM_011514314.1:c.712A>G	XP_011512616.1:p.Ser238Gly
NM_000500.9:c.1117A>G MANE Select	NP_000491.4:p.Ser373Gly
NM_001368143.1:c.712A>G	NP_001355072.1:p.Ser238Gly
NM_001368144.1:c.712A>G	NP_001355073.1:p.Ser238Gly
NM_001128590.4:c.1027A>G	NP_001122062.3:p.Ser343Gly
NM_001368143.2:c.712A>G	NP_001355072.1:p.Ser238Gly
NM_001368144.2:c.712A>G	NP_001355073.1:p.Ser238Gly