Canonical Allele Identifier: CA340728797

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724516T>A (hg19) ; chr1:g.67258833T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258833T>A , CM000663.2:g.67258833T>A	GRCh38
NC_000001.10:g.67724516T>A , CM000663.1:g.67724516T>A	GRCh37
NC_000001.9:g.67497104T>A	NCBI36
NG_011498.1:g.97348T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1434T>A	ENSP00000513138.1:n.1434T>A
ENST00000697150.1:c.1492T>A	ENSP00000513139.1:n.1492T>A
ENST00000697151.1:c.1425T>A	ENSP00000513140.1:n.1425T>A
ENST00000697164.1:c.1505T>A	ENSP00000513153.1:p.Phe502Tyr
ENST00000697165.1:c.1292T>A	ENSP00000513154.1:p.Phe431Tyr
ENST00000347310.10:c.1595T>A MANE Select	ENSP00000321345.5:p.Phe532Tyr
ENST00000637002.1:c.986T>A	ENSP00000490340.1:p.Phe329Tyr
ENST00000347310.9:c.1595T>A	ENSP00000321345.5:p.Phe532Tyr
ENST00000395227.2:c.389T>A	ENSP00000378652.2:p.Phe130Tyr
ENST00000425614.3:c.830T>A	ENSP00000387640.2:p.Phe277Tyr
ENST00000473881.2:c.*421T>A	ENSP00000486667.1:n.*421T>A
NM_144701.2:c.1595T>A	NP_653302.2:p.Phe532Tyr
XM_005270516.2:c.833T>A	XP_005270573.1:p.Phe278Tyr
XM_011540789.1:c.1685T>A	XP_011539091.1:p.Phe562Tyr
XM_011540790.1:c.1595T>A	XP_011539092.1:p.Phe532Tyr
XM_011540791.1:c.1595T>A	XP_011539093.1:p.Phe532Tyr
XM_011540790.3:c.1595T>A	XP_011539092.1:p.Phe532Tyr
XM_011540791.3:c.1595T>A	XP_011539093.1:p.Phe532Tyr
XR_001736993.1:n.1675T>A
NM_144701.3:c.1595T>A MANE Select	NP_653302.2:p.Phe532Tyr