Canonical Allele Identifier: CA418438790

Gene: IL23R

Linked Data

• dbSNP Id: rs1211875196
• gnomAD v2: 1-67724742-T-C
• gnomAD v4: 1-67259059-T-C
• MyVariant Identifiers: chr1:g.67724742T>C (hg19) ; chr1:g.67259059T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259059T>C , CM000663.2:g.67259059T>C	GRCh38
NC_000001.10:g.67724742T>C , CM000663.1:g.67724742T>C	GRCh37
NC_000001.9:g.67497330T>C	NCBI36
NG_011498.1:g.97574T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1660T>C	ENSP00000513138.1:n.1660T>C
ENST00000697150.1:c.1718T>C	ENSP00000513139.1:n.1718T>C
ENST00000697151.1:c.1651T>C	ENSP00000513140.1:n.1651T>C
ENST00000697164.1:c.1731T>C	ENSP00000513153.1:p.Ser577=
ENST00000697165.1:c.1518T>C	ENSP00000513154.1:p.Ser506=
ENST00000347310.10:c.1821T>C MANE Select	ENSP00000321345.5:p.Ser607=
ENST00000637002.1:c.1212T>C	ENSP00000490340.1:p.Ser404=
ENST00000347310.9:c.1821T>C	ENSP00000321345.5:p.Ser607=
ENST00000395227.2:c.615T>C	ENSP00000378652.2:p.Ser205=
ENST00000425614.3:c.1056T>C	ENSP00000387640.2:p.Ser352=
ENST00000473881.2:c.*647T>C	ENSP00000486667.1:n.*647T>C
NM_144701.2:c.1821T>C	NP_653302.2:p.Ser607=
XM_005270516.2:c.1059T>C	XP_005270573.1:p.Ser353=
XM_011540789.1:c.1911T>C	XP_011539091.1:p.Ser637=
XM_011540790.1:c.1821T>C	XP_011539092.1:p.Ser607=
XM_011540791.1:c.1821T>C	XP_011539093.1:p.Ser607=
XM_011540790.3:c.1821T>C	XP_011539092.1:p.Ser607=
XM_011540791.3:c.1821T>C	XP_011539093.1:p.Ser607=
XR_001736993.1:n.1901T>C
NM_144701.3:c.1821T>C MANE Select	NP_653302.2:p.Ser607=