Canonical Allele Identifier: CA340729459

Gene: IL23R

Linked Data

• dbSNP Id: rs1169791532
• gnomAD v2: 1-67724662-A-G
• gnomAD v4: 1-67258979-A-G
• MyVariant Identifiers: chr1:g.67724662A>G (hg19) ; chr1:g.67258979A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258979A>G , CM000663.2:g.67258979A>G	GRCh38
NC_000001.10:g.67724662A>G , CM000663.1:g.67724662A>G	GRCh37
NC_000001.9:g.67497250A>G	NCBI36
NG_011498.1:g.97494A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1580A>G	ENSP00000513138.1:n.1580A>G
ENST00000697150.1:c.1638A>G	ENSP00000513139.1:n.1638A>G
ENST00000697151.1:c.1571A>G	ENSP00000513140.1:n.1571A>G
ENST00000697164.1:c.1651A>G	ENSP00000513153.1:p.Ser551Gly
ENST00000697165.1:c.1438A>G	ENSP00000513154.1:p.Ser480Gly
ENST00000347310.10:c.1741A>G MANE Select	ENSP00000321345.5:p.Ser581Gly
ENST00000637002.1:c.1132A>G	ENSP00000490340.1:p.Ser378Gly
ENST00000347310.9:c.1741A>G	ENSP00000321345.5:p.Ser581Gly
ENST00000395227.2:c.535A>G	ENSP00000378652.2:p.Ser179Gly
ENST00000425614.3:c.976A>G	ENSP00000387640.2:p.Ser326Gly
ENST00000473881.2:c.*567A>G	ENSP00000486667.1:n.*567A>G
NM_144701.2:c.1741A>G	NP_653302.2:p.Ser581Gly
XM_005270516.2:c.979A>G	XP_005270573.1:p.Ser327Gly
XM_011540789.1:c.1831A>G	XP_011539091.1:p.Ser611Gly
XM_011540790.1:c.1741A>G	XP_011539092.1:p.Ser581Gly
XM_011540791.1:c.1741A>G	XP_011539093.1:p.Ser581Gly
XM_011540790.3:c.1741A>G	XP_011539092.1:p.Ser581Gly
XM_011540791.3:c.1741A>G	XP_011539093.1:p.Ser581Gly
XR_001736993.1:n.1821A>G
NM_144701.3:c.1741A>G MANE Select	NP_653302.2:p.Ser581Gly