Canonical Allele Identifier: CA340729397
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258959T>C , CM000663.2:g.67258959T>C GRCh38
NC_000001.10:g.67724642T>C , CM000663.1:g.67724642T>C GRCh37
NC_000001.9:g.67497230T>C NCBI36
NG_011498.1:g.97474T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1560T>C ENSP00000513138.1:n.1560T>C
ENST00000697150.1:c.1618T>C ENSP00000513139.1:n.1618T>C
ENST00000697151.1:c.1551T>C ENSP00000513140.1:n.1551T>C
ENST00000697164.1:c.1631T>C ENSP00000513153.1:p.Leu544Pro
ENST00000697165.1:c.1418T>C ENSP00000513154.1:p.Leu473Pro
ENST00000347310.10:c.1721T>C MANE Select ENSP00000321345.5:p.Leu574Pro
ENST00000637002.1:c.1112T>C ENSP00000490340.1:p.Leu371Pro
ENST00000347310.9:c.1721T>C ENSP00000321345.5:p.Leu574Pro
ENST00000395227.2:c.515T>C ENSP00000378652.2:p.Leu172Pro
ENST00000425614.3:c.956T>C ENSP00000387640.2:p.Leu319Pro
ENST00000473881.2:c.*547T>C ENSP00000486667.1:n.*547T>C
NM_144701.2:c.1721T>C NP_653302.2:p.Leu574Pro
XM_005270516.2:c.959T>C XP_005270573.1:p.Leu320Pro
XM_011540789.1:c.1811T>C XP_011539091.1:p.Leu604Pro
XM_011540790.1:c.1721T>C XP_011539092.1:p.Leu574Pro
XM_011540791.1:c.1721T>C XP_011539093.1:p.Leu574Pro
XM_011540790.3:c.1721T>C XP_011539092.1:p.Leu574Pro
XM_011540791.3:c.1721T>C XP_011539093.1:p.Leu574Pro
XR_001736993.1:n.1801T>C
NM_144701.3:c.1721T>C MANE Select NP_653302.2:p.Leu574Pro