Canonical Allele Identifier: CA340728559

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724420A>C (hg19) ; chr1:g.67258737A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258737A>C , CM000663.2:g.67258737A>C	GRCh38
NC_000001.10:g.67724420A>C , CM000663.1:g.67724420A>C	GRCh37
NC_000001.9:g.67497008A>C	NCBI36
NG_011498.1:g.97252A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1338A>C	ENSP00000513138.1:n.1338A>C
ENST00000697150.1:c.1396A>C	ENSP00000513139.1:n.1396A>C
ENST00000697151.1:c.1329A>C	ENSP00000513140.1:n.1329A>C
ENST00000697164.1:c.1409A>C	ENSP00000513153.1:p.Asn470Thr
ENST00000697165.1:c.1196A>C	ENSP00000513154.1:p.Asn399Thr
ENST00000347310.10:c.1499A>C MANE Select	ENSP00000321345.5:p.Asn500Thr
ENST00000637002.1:c.890A>C	ENSP00000490340.1:p.Asn297Thr
ENST00000347310.9:c.1499A>C	ENSP00000321345.5:p.Asn500Thr
ENST00000395227.2:c.293A>C	ENSP00000378652.2:p.Asn98Thr
ENST00000425614.3:c.734A>C	ENSP00000387640.2:p.Asn245Thr
ENST00000473881.2:c.*325A>C	ENSP00000486667.1:n.*325A>C
NM_144701.2:c.1499A>C	NP_653302.2:p.Asn500Thr
XM_005270516.2:c.737A>C	XP_005270573.1:p.Asn246Thr
XM_011540789.1:c.1589A>C	XP_011539091.1:p.Asn530Thr
XM_011540790.1:c.1499A>C	XP_011539092.1:p.Asn500Thr
XM_011540791.1:c.1499A>C	XP_011539093.1:p.Asn500Thr
XM_011540790.3:c.1499A>C	XP_011539092.1:p.Asn500Thr
XM_011540791.3:c.1499A>C	XP_011539093.1:p.Asn500Thr
XR_001736993.1:n.1579A>C
NM_144701.3:c.1499A>C MANE Select	NP_653302.2:p.Asn500Thr