Canonical Allele Identifier: CA900035
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs756910475
gnomAD v2: 1-67724501-A-G
gnomAD v4: 1-67258818-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258818A>G , CM000663.2:g.67258818A>G GRCh38
NC_000001.10:g.67724501A>G , CM000663.1:g.67724501A>G GRCh37
NC_000001.9:g.67497089A>G NCBI36
NG_011498.1:g.97333A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1419A>G ENSP00000513138.1:n.1419A>G
ENST00000697150.1:c.1477A>G ENSP00000513139.1:n.1477A>G
ENST00000697151.1:c.1410A>G ENSP00000513140.1:n.1410A>G
ENST00000697164.1:c.1490A>G ENSP00000513153.1:p.His497Arg
ENST00000697165.1:c.1277A>G ENSP00000513154.1:p.His426Arg
ENST00000347310.10:c.1580A>G MANE Select ENSP00000321345.5:p.His527Arg
ENST00000637002.1:c.971A>G ENSP00000490340.1:p.His324Arg
ENST00000347310.9:c.1580A>G ENSP00000321345.5:p.His527Arg
ENST00000395227.2:c.374A>G ENSP00000378652.2:p.His125Arg
ENST00000425614.3:c.815A>G ENSP00000387640.2:p.His272Arg
ENST00000473881.2:c.*406A>G ENSP00000486667.1:n.*406A>G
NM_144701.2:c.1580A>G NP_653302.2:p.His527Arg
XM_005270516.2:c.818A>G XP_005270573.1:p.His273Arg
XM_011540789.1:c.1670A>G XP_011539091.1:p.His557Arg
XM_011540790.1:c.1580A>G XP_011539092.1:p.His527Arg
XM_011540791.1:c.1580A>G XP_011539093.1:p.His527Arg
XM_011540790.3:c.1580A>G XP_011539092.1:p.His527Arg
XM_011540791.3:c.1580A>G XP_011539093.1:p.His527Arg
XR_001736993.1:n.1660A>G
NM_144701.3:c.1580A>G MANE Select NP_653302.2:p.His527Arg