Canonical Allele Identifier: CA340728554

Gene: IL23R

Linked Data

• ClinVar Variation Id: 1391966
• ClinVar RCV Id: RCV001893354
• dbSNP Id: rs2100397830
• MyVariant Identifiers: chr1:g.67724419A>G (hg19) ; chr1:g.67258736A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258736A>G , CM000663.2:g.67258736A>G	GRCh38
NC_000001.10:g.67724419A>G , CM000663.1:g.67724419A>G	GRCh37
NC_000001.9:g.67497007A>G	NCBI36
NG_011498.1:g.97251A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1337A>G	ENSP00000513138.1:n.1337A>G
ENST00000697150.1:c.1395A>G	ENSP00000513139.1:n.1395A>G
ENST00000697151.1:c.1328A>G	ENSP00000513140.1:n.1328A>G
ENST00000697164.1:c.1408A>G	ENSP00000513153.1:p.Asn470Asp
ENST00000697165.1:c.1195A>G	ENSP00000513154.1:p.Asn399Asp
ENST00000347310.10:c.1498A>G MANE Select	ENSP00000321345.5:p.Asn500Asp
ENST00000637002.1:c.889A>G	ENSP00000490340.1:p.Asn297Asp
ENST00000347310.9:c.1498A>G	ENSP00000321345.5:p.Asn500Asp
ENST00000395227.2:c.292A>G	ENSP00000378652.2:p.Asn98Asp
ENST00000425614.3:c.733A>G	ENSP00000387640.2:p.Asn245Asp
ENST00000473881.2:c.*324A>G	ENSP00000486667.1:n.*324A>G
NM_144701.2:c.1498A>G	NP_653302.2:p.Asn500Asp
XM_005270516.2:c.736A>G	XP_005270573.1:p.Asn246Asp
XM_011540789.1:c.1588A>G	XP_011539091.1:p.Asn530Asp
XM_011540790.1:c.1498A>G	XP_011539092.1:p.Asn500Asp
XM_011540791.1:c.1498A>G	XP_011539093.1:p.Asn500Asp
XM_011540790.3:c.1498A>G	XP_011539092.1:p.Asn500Asp
XM_011540791.3:c.1498A>G	XP_011539093.1:p.Asn500Asp
XR_001736993.1:n.1578A>G
NM_144701.3:c.1498A>G MANE Select	NP_653302.2:p.Asn500Asp