Canonical Allele Identifier: CA340728710
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258796A>C , CM000663.2:g.67258796A>C GRCh38
NC_000001.10:g.67724479A>C , CM000663.1:g.67724479A>C GRCh37
NC_000001.9:g.67497067A>C NCBI36
NG_011498.1:g.97311A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1397A>C ENSP00000513138.1:n.1397A>C
ENST00000697150.1:c.1455A>C ENSP00000513139.1:n.1455A>C
ENST00000697151.1:c.1388A>C ENSP00000513140.1:n.1388A>C
ENST00000697164.1:c.1468A>C ENSP00000513153.1:p.Asn490His
ENST00000697165.1:c.1255A>C ENSP00000513154.1:p.Asn419His
ENST00000347310.10:c.1558A>C MANE Select ENSP00000321345.5:p.Asn520His
ENST00000637002.1:c.949A>C ENSP00000490340.1:p.Asn317His
ENST00000347310.9:c.1558A>C ENSP00000321345.5:p.Asn520His
ENST00000395227.2:c.352A>C ENSP00000378652.2:p.Asn118His
ENST00000425614.3:c.793A>C ENSP00000387640.2:p.Asn265His
ENST00000473881.2:c.*384A>C ENSP00000486667.1:n.*384A>C
NM_144701.2:c.1558A>C NP_653302.2:p.Asn520His
XM_005270516.2:c.796A>C XP_005270573.1:p.Asn266His
XM_011540789.1:c.1648A>C XP_011539091.1:p.Asn550His
XM_011540790.1:c.1558A>C XP_011539092.1:p.Asn520His
XM_011540791.1:c.1558A>C XP_011539093.1:p.Asn520His
XM_011540790.3:c.1558A>C XP_011539092.1:p.Asn520His
XM_011540791.3:c.1558A>C XP_011539093.1:p.Asn520His
XR_001736993.1:n.1638A>C
NM_144701.3:c.1558A>C MANE Select NP_653302.2:p.Asn520His