Canonical Allele Identifier: CA900031
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs373245679
gnomAD v2: 1-67724473-T-C
gnomAD v3: 1-67258790-T-C
gnomAD v4: 1-67258790-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258790T>C , CM000663.2:g.67258790T>C GRCh38
NC_000001.10:g.67724473T>C , CM000663.1:g.67724473T>C GRCh37
NC_000001.9:g.67497061T>C NCBI36
NG_011498.1:g.97305T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1391T>C ENSP00000513138.1:n.1391T>C
ENST00000697150.1:c.1449T>C ENSP00000513139.1:n.1449T>C
ENST00000697151.1:c.1382T>C ENSP00000513140.1:n.1382T>C
ENST00000697164.1:c.1462T>C ENSP00000513153.1:p.Ser488Pro
ENST00000697165.1:c.1249T>C ENSP00000513154.1:p.Ser417Pro
ENST00000347310.10:c.1552T>C MANE Select ENSP00000321345.5:p.Ser518Pro
ENST00000637002.1:c.943T>C ENSP00000490340.1:p.Ser315Pro
ENST00000347310.9:c.1552T>C ENSP00000321345.5:p.Ser518Pro
ENST00000395227.2:c.346T>C ENSP00000378652.2:p.Ser116Pro
ENST00000425614.3:c.787T>C ENSP00000387640.2:p.Ser263Pro
ENST00000473881.2:c.*378T>C ENSP00000486667.1:n.*378T>C
NM_144701.2:c.1552T>C NP_653302.2:p.Ser518Pro
XM_005270516.2:c.790T>C XP_005270573.1:p.Ser264Pro
XM_011540789.1:c.1642T>C XP_011539091.1:p.Ser548Pro
XM_011540790.1:c.1552T>C XP_011539092.1:p.Ser518Pro
XM_011540791.1:c.1552T>C XP_011539093.1:p.Ser518Pro
XM_011540790.3:c.1552T>C XP_011539092.1:p.Ser518Pro
XM_011540791.3:c.1552T>C XP_011539093.1:p.Ser518Pro
XR_001736993.1:n.1632T>C
NM_144701.3:c.1552T>C MANE Select NP_653302.2:p.Ser518Pro