Canonical Allele Identifier: CA900038
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs756596999
gnomAD v2: 1-67724520-T-C
gnomAD v3: 1-67258837-T-C
gnomAD v4: 1-67258837-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258837T>C , CM000663.2:g.67258837T>C GRCh38
NC_000001.10:g.67724520T>C , CM000663.1:g.67724520T>C GRCh37
NC_000001.9:g.67497108T>C NCBI36
NG_011498.1:g.97352T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1438T>C ENSP00000513138.1:n.1438T>C
ENST00000697150.1:c.1496T>C ENSP00000513139.1:n.1496T>C
ENST00000697151.1:c.1429T>C ENSP00000513140.1:n.1429T>C
ENST00000697164.1:c.1509T>C ENSP00000513153.1:p.Ser503=
ENST00000697165.1:c.1296T>C ENSP00000513154.1:p.Ser432=
ENST00000347310.10:c.1599T>C MANE Select ENSP00000321345.5:p.Ser533=
ENST00000637002.1:c.990T>C ENSP00000490340.1:p.Ser330=
ENST00000347310.9:c.1599T>C ENSP00000321345.5:p.Ser533=
ENST00000395227.2:c.393T>C ENSP00000378652.2:p.Ser131=
ENST00000425614.3:c.834T>C ENSP00000387640.2:p.Ser278=
ENST00000473881.2:c.*425T>C ENSP00000486667.1:n.*425T>C
NM_144701.2:c.1599T>C NP_653302.2:p.Ser533=
XM_005270516.2:c.837T>C XP_005270573.1:p.Ser279=
XM_011540789.1:c.1689T>C XP_011539091.1:p.Ser563=
XM_011540790.1:c.1599T>C XP_011539092.1:p.Ser533=
XM_011540791.1:c.1599T>C XP_011539093.1:p.Ser533=
XM_011540790.3:c.1599T>C XP_011539092.1:p.Ser533=
XM_011540791.3:c.1599T>C XP_011539093.1:p.Ser533=
XR_001736993.1:n.1679T>C
NM_144701.3:c.1599T>C MANE Select NP_653302.2:p.Ser533=