Canonical Allele Identifier: CA340729798
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259066A>C , CM000663.2:g.67259066A>C GRCh38
NC_000001.10:g.67724749A>C , CM000663.1:g.67724749A>C GRCh37
NC_000001.9:g.67497337A>C NCBI36
NG_011498.1:g.97581A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1667A>C ENSP00000513138.1:n.1667A>C
ENST00000697150.1:c.1725A>C ENSP00000513139.1:n.1725A>C
ENST00000697151.1:c.1658A>C ENSP00000513140.1:n.1658A>C
ENST00000697164.1:c.1738A>C ENSP00000513153.1:p.Thr580Pro
ENST00000697165.1:c.1525A>C ENSP00000513154.1:p.Thr509Pro
ENST00000347310.10:c.1828A>C MANE Select ENSP00000321345.5:p.Thr610Pro
ENST00000637002.1:c.1219A>C ENSP00000490340.1:p.Thr407Pro
ENST00000347310.9:c.1828A>C ENSP00000321345.5:p.Thr610Pro
ENST00000395227.2:c.622A>C ENSP00000378652.2:p.Thr208Pro
ENST00000425614.3:c.1063A>C ENSP00000387640.2:p.Thr355Pro
ENST00000473881.2:c.*654A>C ENSP00000486667.1:n.*654A>C
NM_144701.2:c.1828A>C NP_653302.2:p.Thr610Pro
XM_005270516.2:c.1066A>C XP_005270573.1:p.Thr356Pro
XM_011540789.1:c.1918A>C XP_011539091.1:p.Thr640Pro
XM_011540790.1:c.1828A>C XP_011539092.1:p.Thr610Pro
XM_011540791.1:c.1828A>C XP_011539093.1:p.Thr610Pro
XM_011540790.3:c.1828A>C XP_011539092.1:p.Thr610Pro
XM_011540791.3:c.1828A>C XP_011539093.1:p.Thr610Pro
XR_001736993.1:n.1908A>C
NM_144701.3:c.1828A>C MANE Select NP_653302.2:p.Thr610Pro