Canonical Allele Identifier: CA23506286

Gene: IL23R

Linked Data

• dbSNP Id: rs886133623
• gnomAD v2: 1-67724437-T-G
• gnomAD v3: 1-67258754-T-G
• gnomAD v4: 1-67258754-T-G
• MyVariant Identifiers: chr1:g.67724437T>G (hg19) ; chr1:g.67258754T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258754T>G , CM000663.2:g.67258754T>G	GRCh38
NC_000001.10:g.67724437T>G , CM000663.1:g.67724437T>G	GRCh37
NC_000001.9:g.67497025T>G	NCBI36
NG_011498.1:g.97269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1355T>G	ENSP00000513138.1:n.1355T>G
ENST00000697150.1:c.1413T>G	ENSP00000513139.1:n.1413T>G
ENST00000697151.1:c.1346T>G	ENSP00000513140.1:n.1346T>G
ENST00000697164.1:c.1426T>G	ENSP00000513153.1:p.Ser476Ala
ENST00000697165.1:c.1213T>G	ENSP00000513154.1:p.Ser405Ala
ENST00000347310.10:c.1516T>G MANE Select	ENSP00000321345.5:p.Ser506Ala
ENST00000637002.1:c.907T>G	ENSP00000490340.1:p.Ser303Ala
ENST00000347310.9:c.1516T>G	ENSP00000321345.5:p.Ser506Ala
ENST00000395227.2:c.310T>G	ENSP00000378652.2:p.Ser104Ala
ENST00000425614.3:c.751T>G	ENSP00000387640.2:p.Ser251Ala
ENST00000473881.2:c.*342T>G	ENSP00000486667.1:n.*342T>G
NM_144701.2:c.1516T>G	NP_653302.2:p.Ser506Ala
XM_005270516.2:c.754T>G	XP_005270573.1:p.Ser252Ala
XM_011540789.1:c.1606T>G	XP_011539091.1:p.Ser536Ala
XM_011540790.1:c.1516T>G	XP_011539092.1:p.Ser506Ala
XM_011540791.1:c.1516T>G	XP_011539093.1:p.Ser506Ala
XM_011540790.3:c.1516T>G	XP_011539092.1:p.Ser506Ala
XM_011540791.3:c.1516T>G	XP_011539093.1:p.Ser506Ala
XR_001736993.1:n.1596T>G
NM_144701.3:c.1516T>G MANE Select	NP_653302.2:p.Ser506Ala