Canonical Allele Identifier: CA340728714
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258797A>T , CM000663.2:g.67258797A>T GRCh38
NC_000001.10:g.67724480A>T , CM000663.1:g.67724480A>T GRCh37
NC_000001.9:g.67497068A>T NCBI36
NG_011498.1:g.97312A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1398A>T ENSP00000513138.1:n.1398A>T
ENST00000697150.1:c.1456A>T ENSP00000513139.1:n.1456A>T
ENST00000697151.1:c.1389A>T ENSP00000513140.1:n.1389A>T
ENST00000697164.1:c.1469A>T ENSP00000513153.1:p.Asn490Ile
ENST00000697165.1:c.1256A>T ENSP00000513154.1:p.Asn419Ile
ENST00000347310.10:c.1559A>T MANE Select ENSP00000321345.5:p.Asn520Ile
ENST00000637002.1:c.950A>T ENSP00000490340.1:p.Asn317Ile
ENST00000347310.9:c.1559A>T ENSP00000321345.5:p.Asn520Ile
ENST00000395227.2:c.353A>T ENSP00000378652.2:p.Asn118Ile
ENST00000425614.3:c.794A>T ENSP00000387640.2:p.Asn265Ile
ENST00000473881.2:c.*385A>T ENSP00000486667.1:n.*385A>T
NM_144701.2:c.1559A>T NP_653302.2:p.Asn520Ile
XM_005270516.2:c.797A>T XP_005270573.1:p.Asn266Ile
XM_011540789.1:c.1649A>T XP_011539091.1:p.Asn550Ile
XM_011540790.1:c.1559A>T XP_011539092.1:p.Asn520Ile
XM_011540791.1:c.1559A>T XP_011539093.1:p.Asn520Ile
XM_011540790.3:c.1559A>T XP_011539092.1:p.Asn520Ile
XM_011540791.3:c.1559A>T XP_011539093.1:p.Asn520Ile
XR_001736993.1:n.1639A>T
NM_144701.3:c.1559A>T MANE Select NP_653302.2:p.Asn520Ile