Canonical Allele Identifier: CA340725730
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240179A>G , CM000663.2:g.67240179A>G GRCh38
NC_000001.10:g.67705862A>G , CM000663.1:g.67705862A>G GRCh37
NC_000001.9:g.67478450A>G NCBI36
NG_011498.1:g.78694A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.922A>G ENSP00000513137.1:n.922A>G
ENST00000697149.1:c.885A>G ENSP00000513138.1:n.885A>G
ENST00000697150.1:c.1045+3377A>G ENSP00000513139.1:n.1045+3377A>G
ENST00000697151.1:c.1045+3377A>G ENSP00000513140.1:n.1045+3377A>G
ENST00000697152.1:c.799-15658A>G ENSP00000513141.1:n.799-15658A>G
ENST00000697153.1:c.795-15658A>G ENSP00000513142.1:n.795-15658A>G
ENST00000697154.1:c.956-18299A>G ENSP00000513143.1:n.956-18299A>G
ENST00000697155.1:c.649-18299A>G ENSP00000513144.1:n.649-18299A>G
ENST00000697156.1:c.1046A>G ENSP00000513145.1:p.Asp349Gly
ENST00000697157.1:c.900A>G ENSP00000513146.1:n.900A>G
ENST00000697158.1:c.889A>G ENSP00000513147.1:n.889A>G
ENST00000697159.1:c.739A>G ENSP00000513148.1:n.739A>G
ENST00000697160.1:c.956-15658A>G ENSP00000513149.1:n.956-15658A>G
ENST00000697161.1:c.582A>G ENSP00000513150.1:n.582A>G
ENST00000697162.1:c.975A>G ENSP00000513151.1:n.975A>G
ENST00000697163.1:c.1046A>G ENSP00000513152.1:p.Asp349Gly
ENST00000697164.1:c.956A>G ENSP00000513153.1:p.Asp319Gly
ENST00000697165.1:c.743A>G ENSP00000513154.1:p.Asp248Gly
ENST00000697223.1:c.795A>G ENSP00000513190.1:n.795A>G
ENST00000697224.1:c.884+3377A>G ENSP00000513191.1:n.884+3377A>G
ENST00000697225.1:c.649A>G ENSP00000513192.1:n.649A>G
ENST00000697226.1:c.738+3377A>G ENSP00000513193.1:n.738+3377A>G
ENST00000697227.1:c.882A>G ENSP00000513194.1:p.Ter294Trp
ENST00000697228.1:c.738A>G ENSP00000513195.1:n.738A>G
ENST00000697229.1:c.885-15658A>G ENSP00000513196.1:n.885-15658A>G
ENST00000697230.1:c.956A>G ENSP00000513197.1:p.Asp319Gly
ENST00000697231.1:c.951A>G ENSP00000513198.1:n.951A>G
ENST00000697232.1:c.975A>G ENSP00000513199.1:n.975A>G
ENST00000347310.10:c.1046A>G MANE Select ENSP00000321345.5:p.Asp349Gly
ENST00000637002.1:c.437A>G ENSP00000490340.1:p.Asp146Gly
ENST00000347310.9:c.1046A>G ENSP00000321345.5:p.Asp349Gly
ENST00000395227.2:c.-58-15658A>G ENSP00000378652.2:n.-58-15658A>G
ENST00000425614.3:c.281A>G ENSP00000387640.2:p.Asp94Gly
ENST00000473881.2:c.191-15658A>G ENSP00000486667.1:n.191-15658A>G
NM_144701.2:c.1046A>G NP_653302.2:p.Asp349Gly
XM_005270516.2:c.284A>G XP_005270573.1:p.Asp95Gly
XM_011540789.1:c.1136A>G XP_011539091.1:p.Asp379Gly
XM_011540790.1:c.1046A>G XP_011539092.1:p.Asp349Gly
XM_011540791.1:c.1046A>G XP_011539093.1:p.Asp349Gly
XM_011540790.3:c.1046A>G XP_011539092.1:p.Asp349Gly
XM_011540791.3:c.1046A>G XP_011539093.1:p.Asp349Gly
XR_001736993.1:n.1228+3377A>G
NM_144701.3:c.1046A>G MANE Select NP_653302.2:p.Asp349Gly