Canonical Allele Identifier: CA363502270

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1776073674
• gnomAD v4: 6-32039248-G-C
• MyVariant Identifiers: chr6:g.32007025G>C (hg19) ; chr6:g.32039248G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039248G>C , CM000668.2:g.32039248G>C	GRCh38
NC_000006.11:g.32007025G>C , CM000668.1:g.32007025G>C	GRCh37
NC_000006.10:g.32115004G>C	NCBI36
NG_007941.2:g.5941G>C
NG_008337.2:g.75127C>G
NG_007941.3:g.5944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.447G>C MANE Select	ENSP00000496625.1:p.Glu149Asp
ENST00000418967.6:c.447G>C	ENSP00000408860.2:p.Glu149Asp
ENST00000435122.3:c.357G>C	ENSP00000415043.2:p.Glu119Asp
ENST00000462278.1:n.35G>C
ENST00000464325.5:n.368G>C
ENST00000466779.5:c.*139G>C	ENSP00000417321.1:n.*139G>C
ENST00000466879.5:n.498G>C
ENST00000469053.5:c.*139G>C	ENSP00000418104.1:n.*139G>C
ENST00000471671.4:c.447G>C	ENSP00000418561.1:p.Glu149Asp
ENST00000478281.5:c.480G>C	ENSP00000419572.1:p.Glu160Asp
ENST00000479074.5:n.505G>C
ENST00000479730.5:n.602G>C
ENST00000483041.5:n.616G>C
ENST00000486063.5:n.627G>C
ENST00000488465.1:n.455G>C
NM_000500.7:c.447G>C	NP_000491.4:p.Glu149Asp
NM_001128590.3:c.357G>C	NP_001122062.3:p.Glu119Asp
XM_011514314.1:c.42G>C	XP_011512616.1:p.Glu14Asp
NM_000500.9:c.447G>C MANE Select	NP_000491.4:p.Glu149Asp
NM_001368143.1:c.42G>C	NP_001355072.1:p.Glu14Asp
NM_001368144.1:c.42G>C	NP_001355073.1:p.Glu14Asp
NM_001128590.4:c.357G>C	NP_001122062.3:p.Glu119Asp
NM_001368143.2:c.42G>C	NP_001355072.1:p.Glu14Asp
NM_001368144.2:c.42G>C	NP_001355073.1:p.Glu14Asp