Canonical Allele Identifier: CA340728914
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258864C>G , CM000663.2:g.67258864C>G GRCh38
NC_000001.10:g.67724547C>G , CM000663.1:g.67724547C>G GRCh37
NC_000001.9:g.67497135C>G NCBI36
NG_011498.1:g.97379C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1465C>G ENSP00000513138.1:n.1465C>G
ENST00000697150.1:c.1523C>G ENSP00000513139.1:n.1523C>G
ENST00000697151.1:c.1456C>G ENSP00000513140.1:n.1456C>G
ENST00000697164.1:c.1536C>G ENSP00000513153.1:p.Asn512Lys
ENST00000697165.1:c.1323C>G ENSP00000513154.1:p.Asn441Lys
ENST00000347310.10:c.1626C>G MANE Select ENSP00000321345.5:p.Asn542Lys
ENST00000637002.1:c.1017C>G ENSP00000490340.1:p.Asn339Lys
ENST00000347310.9:c.1626C>G ENSP00000321345.5:p.Asn542Lys
ENST00000395227.2:c.420C>G ENSP00000378652.2:p.Asn140Lys
ENST00000425614.3:c.861C>G ENSP00000387640.2:p.Asn287Lys
ENST00000473881.2:c.*452C>G ENSP00000486667.1:n.*452C>G
NM_144701.2:c.1626C>G NP_653302.2:p.Asn542Lys
XM_005270516.2:c.864C>G XP_005270573.1:p.Asn288Lys
XM_011540789.1:c.1716C>G XP_011539091.1:p.Asn572Lys
XM_011540790.1:c.1626C>G XP_011539092.1:p.Asn542Lys
XM_011540791.1:c.1626C>G XP_011539093.1:p.Asn542Lys
XM_011540790.3:c.1626C>G XP_011539092.1:p.Asn542Lys
XM_011540791.3:c.1626C>G XP_011539093.1:p.Asn542Lys
XR_001736993.1:n.1706C>G
NM_144701.3:c.1626C>G MANE Select NP_653302.2:p.Asn542Lys