Canonical Allele Identifier: CA418438742

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724505T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258822T>C , CM000663.2:g.67258822T>C	GRCh38
NC_000001.10:g.67724505T>C , CM000663.1:g.67724505T>C	GRCh37
NC_000001.9:g.67497093T>C	NCBI36
NG_011498.1:g.97337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1423T>C	ENSP00000513138.1:n.1423T>C
ENST00000697150.1:c.1481T>C	ENSP00000513139.1:n.1481T>C
ENST00000697151.1:c.1414T>C	ENSP00000513140.1:n.1414T>C
ENST00000697164.1:c.1494T>C	ENSP00000513153.1:p.Pro498=
ENST00000697165.1:c.1281T>C	ENSP00000513154.1:p.Pro427=
ENST00000347310.10:c.1584T>C MANE Select	ENSP00000321345.5:p.Pro528=
ENST00000637002.1:c.975T>C	ENSP00000490340.1:p.Pro325=
ENST00000347310.9:c.1584T>C	ENSP00000321345.5:p.Pro528=
ENST00000395227.2:c.378T>C	ENSP00000378652.2:p.Pro126=
ENST00000425614.3:c.819T>C	ENSP00000387640.2:p.Pro273=
ENST00000473881.2:c.*410T>C	ENSP00000486667.1:n.*410T>C
NM_144701.2:c.1584T>C	NP_653302.2:p.Pro528=
XM_005270516.2:c.822T>C	XP_005270573.1:p.Pro274=
XM_011540789.1:c.1674T>C	XP_011539091.1:p.Pro558=
XM_011540790.1:c.1584T>C	XP_011539092.1:p.Pro528=
XM_011540791.1:c.1584T>C	XP_011539093.1:p.Pro528=
XM_011540790.3:c.1584T>C	XP_011539092.1:p.Pro528=
XM_011540791.3:c.1584T>C	XP_011539093.1:p.Pro528=
XR_001736993.1:n.1664T>C
NM_144701.3:c.1584T>C MANE Select	NP_653302.2:p.Pro528=