Canonical Allele Identifier: CA363501324

Gene: CYP21A2

Linked Data

• ClinVar Variation Id: 375321
• ClinVar RCV Id: RCV001865312
• dbSNP Id: rs1057519069
• MyVariant Identifiers: chr6:g.32006955C>G (hg19) ; chr6:g.32039178C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039178C>G , CM000668.2:g.32039178C>G	GRCh38
NC_000006.11:g.32006955C>G , CM000668.1:g.32006955C>G	GRCh37
NC_000006.10:g.32114934C>G	NCBI36
NG_007941.2:g.5871C>G
NG_008337.2:g.75197G>C
NG_007941.3:g.5874C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.377C>G MANE Select	ENSP00000496625.1:p.Ser126Ter
ENST00000418967.6:c.377C>G	ENSP00000408860.2:p.Ser126Ter
ENST00000435122.3:c.287C>G	ENSP00000415043.2:p.Ser96Ter
ENST00000464325.5:n.298C>G
ENST00000466779.5:c.*69C>G	ENSP00000417321.1:n.*69C>G
ENST00000466879.5:n.428C>G
ENST00000469053.5:c.*69C>G	ENSP00000418104.1:n.*69C>G
ENST00000471671.4:c.377C>G	ENSP00000418561.1:p.Ser126Ter
ENST00000478281.5:c.410C>G	ENSP00000419572.1:p.Ser137Ter
ENST00000479074.5:n.435C>G
ENST00000479730.5:n.532C>G
ENST00000483041.5:n.546C>G
ENST00000486063.5:n.557C>G
ENST00000488465.1:n.385C>G
NM_000500.7:c.377C>G	NP_000491.4:p.Ser126Ter
NM_001128590.3:c.287C>G	NP_001122062.3:p.Ser96Ter
XM_011514314.1:c.-29C>G	XP_011512616.1:n.-29C>G
NM_000500.9:c.377C>G MANE Select	NP_000491.4:p.Ser126Ter
NM_001368143.1:c.-29C>G	NP_001355072.1:n.-29C>G
NM_001368144.1:c.-29C>G	NP_001355073.1:n.-29C>G
NM_001128590.4:c.287C>G	NP_001122062.3:p.Ser96Ter
NM_001368143.2:c.-29C>G	NP_001355072.1:n.-29C>G
NM_001368144.2:c.-29C>G	NP_001355073.1:n.-29C>G