Canonical Allele Identifier: CA900026

Gene: IL23R

Linked Data

• ClinVar Variation Id: 1001726
• ClinVar RCV Id: RCV001298059
• dbSNP Id: rs748364447
• ExAC: 1:67724426 A / G
• gnomAD v2: 1-67724426-A-G
• gnomAD v3: 1-67258743-A-G
• gnomAD v4: 1-67258743-A-G
• MyVariant Identifiers: chr1:g.67724426A>G (hg19) ; chr1:g.67258743A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258743A>G , CM000663.2:g.67258743A>G	GRCh38
NC_000001.10:g.67724426A>G , CM000663.1:g.67724426A>G	GRCh37
NC_000001.9:g.67497014A>G	NCBI36
NG_011498.1:g.97258A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1344A>G	ENSP00000513138.1:n.1344A>G
ENST00000697150.1:c.1402A>G	ENSP00000513139.1:n.1402A>G
ENST00000697151.1:c.1335A>G	ENSP00000513140.1:n.1335A>G
ENST00000697164.1:c.1415A>G	ENSP00000513153.1:p.Asn472Ser
ENST00000697165.1:c.1202A>G	ENSP00000513154.1:p.Asn401Ser
ENST00000347310.10:c.1505A>G MANE Select	ENSP00000321345.5:p.Asn502Ser
ENST00000637002.1:c.896A>G	ENSP00000490340.1:p.Asn299Ser
ENST00000347310.9:c.1505A>G	ENSP00000321345.5:p.Asn502Ser
ENST00000395227.2:c.299A>G	ENSP00000378652.2:p.Asn100Ser
ENST00000425614.3:c.740A>G	ENSP00000387640.2:p.Asn247Ser
ENST00000473881.2:c.*331A>G	ENSP00000486667.1:n.*331A>G
NM_144701.2:c.1505A>G	NP_653302.2:p.Asn502Ser
XM_005270516.2:c.743A>G	XP_005270573.1:p.Asn248Ser
XM_011540789.1:c.1595A>G	XP_011539091.1:p.Asn532Ser
XM_011540790.1:c.1505A>G	XP_011539092.1:p.Asn502Ser
XM_011540791.1:c.1505A>G	XP_011539093.1:p.Asn502Ser
XM_011540790.3:c.1505A>G	XP_011539092.1:p.Asn502Ser
XM_011540791.3:c.1505A>G	XP_011539093.1:p.Asn502Ser
XR_001736993.1:n.1585A>G
NM_144701.3:c.1505A>G MANE Select	NP_653302.2:p.Asn502Ser