Canonical Allele Identifier: CA363503058

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32039429-G-C
• MyVariant Identifiers: chr6:g.32007206G>C (hg19) ; chr6:g.32039429G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039429G>C , CM000668.2:g.32039429G>C	GRCh38
NC_000006.11:g.32007206G>C , CM000668.1:g.32007206G>C	GRCh37
NC_000006.10:g.32115185G>C	NCBI36
NG_007941.2:g.6122G>C
NG_008337.2:g.74946C>G
NG_007941.3:g.6125G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.521G>C MANE Select	ENSP00000496625.1:p.Cys174Ser
ENST00000418967.6:c.521G>C	ENSP00000408860.2:p.Cys174Ser
ENST00000435122.3:c.431G>C	ENSP00000415043.2:p.Cys144Ser
ENST00000462278.1:n.109G>C
ENST00000464325.5:n.442G>C
ENST00000466779.5:c.*213G>C	ENSP00000417321.1:n.*213G>C
ENST00000466879.5:n.572G>C
ENST00000469053.5:c.*213G>C	ENSP00000418104.1:n.*213G>C
ENST00000471671.4:c.521G>C	ENSP00000418561.1:p.Cys174Ser
ENST00000478281.5:c.554G>C	ENSP00000419572.1:p.Cys185Ser
ENST00000479074.5:n.579G>C
ENST00000479730.5:n.676G>C
ENST00000483041.5:n.690G>C
ENST00000486063.5:n.701G>C
ENST00000488465.1:n.529G>C
NM_000500.7:c.521G>C	NP_000491.4:p.Cys174Ser
NM_001128590.3:c.431G>C	NP_001122062.3:p.Cys144Ser
XM_011514314.1:c.116G>C	XP_011512616.1:p.Cys39Ser
NM_000500.9:c.521G>C MANE Select	NP_000491.4:p.Cys174Ser
NM_001368143.1:c.116G>C	NP_001355072.1:p.Cys39Ser
NM_001368144.1:c.116G>C	NP_001355073.1:p.Cys39Ser
NM_001128590.4:c.431G>C	NP_001122062.3:p.Cys144Ser
NM_001368143.2:c.116G>C	NP_001355072.1:p.Cys39Ser
NM_001368144.2:c.116G>C	NP_001355073.1:p.Cys39Ser