Canonical Allele Identifier: CA900050

Gene: IL23R

Linked Data

• ClinVar Variation Id: 3002688
• ClinVar RCV Id: RCV003860279
• dbSNP Id: rs768272736
• ExAC: 1:67724663 G / C
• gnomAD v2: 1-67724663-G-C
• gnomAD v3: 1-67258980-G-C
• gnomAD v4: 1-67258980-G-C
• MyVariant Identifiers: chr1:g.67724663G>C (hg19) ; chr1:g.67258980G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258980G>C , CM000663.2:g.67258980G>C	GRCh38
NC_000001.10:g.67724663G>C , CM000663.1:g.67724663G>C	GRCh37
NC_000001.9:g.67497251G>C	NCBI36
NG_011498.1:g.97495G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1581G>C	ENSP00000513138.1:n.1581G>C
ENST00000697150.1:c.1639G>C	ENSP00000513139.1:n.1639G>C
ENST00000697151.1:c.1572G>C	ENSP00000513140.1:n.1572G>C
ENST00000697164.1:c.1652G>C	ENSP00000513153.1:p.Ser551Thr
ENST00000697165.1:c.1439G>C	ENSP00000513154.1:p.Ser480Thr
ENST00000347310.10:c.1742G>C MANE Select	ENSP00000321345.5:p.Ser581Thr
ENST00000637002.1:c.1133G>C	ENSP00000490340.1:p.Ser378Thr
ENST00000347310.9:c.1742G>C	ENSP00000321345.5:p.Ser581Thr
ENST00000395227.2:c.536G>C	ENSP00000378652.2:p.Ser179Thr
ENST00000425614.3:c.977G>C	ENSP00000387640.2:p.Ser326Thr
ENST00000473881.2:c.*568G>C	ENSP00000486667.1:n.*568G>C
NM_144701.2:c.1742G>C	NP_653302.2:p.Ser581Thr
XM_005270516.2:c.980G>C	XP_005270573.1:p.Ser327Thr
XM_011540789.1:c.1832G>C	XP_011539091.1:p.Ser611Thr
XM_011540790.1:c.1742G>C	XP_011539092.1:p.Ser581Thr
XM_011540791.1:c.1742G>C	XP_011539093.1:p.Ser581Thr
XM_011540790.3:c.1742G>C	XP_011539092.1:p.Ser581Thr
XM_011540791.3:c.1742G>C	XP_011539093.1:p.Ser581Thr
XR_001736993.1:n.1822G>C
NM_144701.3:c.1742G>C MANE Select	NP_653302.2:p.Ser581Thr