Canonical Allele Identifier: CA23556498

Gene: IL23R

Linked Data

• dbSNP Id: rs1003608173
• gnomAD v3: 1-67236861-C-G
• gnomAD v4: 1-67236861-C-G
• MyVariant Identifiers: chr1:g.67702544C>G (hg19) ; chr1:g.67236861C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67236861C>G , CM000663.2:g.67236861C>G	GRCh38
NC_000001.10:g.67702544C>G , CM000663.1:g.67702544C>G	GRCh37
NC_000001.9:g.67475132C>G	NCBI36
NG_011498.1:g.75376C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.921+59C>G	ENSP00000513137.1:n.921+59C>G
ENST00000697149.1:c.884+59C>G	ENSP00000513138.1:n.884+59C>G
ENST00000697150.1:c.1045+59C>G	ENSP00000513139.1:n.1045+59C>G
ENST00000697151.1:c.1045+59C>G	ENSP00000513140.1:n.1045+59C>G
ENST00000697152.1:c.799-18976C>G	ENSP00000513141.1:n.799-18976C>G
ENST00000697153.1:c.794+17131C>G	ENSP00000513142.1:n.794+17131C>G
ENST00000697154.1:c.955+17131C>G	ENSP00000513143.1:n.955+17131C>G
ENST00000697155.1:c.648+17131C>G	ENSP00000513144.1:n.648+17131C>G
ENST00000697156.1:c.1045+59C>G	ENSP00000513145.1:n.1045+59C>G
ENST00000697157.1:c.899+59C>G	ENSP00000513146.1:n.899+59C>G
ENST00000697158.1:c.888+59C>G	ENSP00000513147.1:n.888+59C>G
ENST00000697159.1:c.738+59C>G	ENSP00000513148.1:n.738+59C>G
ENST00000697160.1:c.955+17131C>G	ENSP00000513149.1:n.955+17131C>G
ENST00000697161.1:c.581+59C>G	ENSP00000513150.1:n.581+59C>G
ENST00000697162.1:c.974+59C>G	ENSP00000513151.1:n.974+59C>G
ENST00000697163.1:c.1045+59C>G	ENSP00000513152.1:n.1045+59C>G
ENST00000697164.1:c.956-3318C>G	ENSP00000513153.1:n.956-3318C>G
ENST00000697165.1:c.742+59C>G	ENSP00000513154.1:n.742+59C>G
ENST00000697223.1:c.795-3318C>G	ENSP00000513190.1:n.795-3318C>G
ENST00000697224.1:c.884+59C>G	ENSP00000513191.1:n.884+59C>G
ENST00000697225.1:c.649-3318C>G	ENSP00000513192.1:n.649-3318C>G
ENST00000697226.1:c.738+59C>G	ENSP00000513193.1:n.738+59C>G
ENST00000697227.1:c.881+59C>G	ENSP00000513194.1:n.881+59C>G
ENST00000697228.1:c.737+59C>G	ENSP00000513195.1:n.737+59C>G
ENST00000697229.1:c.884+17131C>G	ENSP00000513196.1:n.884+17131C>G
ENST00000697230.1:c.956-3318C>G	ENSP00000513197.1:n.956-3318C>G
ENST00000697231.1:c.951-3318C>G	ENSP00000513198.1:n.951-3318C>G
ENST00000697232.1:c.974+59C>G	ENSP00000513199.1:n.974+59C>G
ENST00000347310.10:c.1045+59C>G MANE Select	ENSP00000321345.5:n.1045+59C>G
ENST00000637002.1:c.436+59C>G	ENSP00000490340.1:n.436+59C>G
ENST00000347310.9:c.1045+59C>G	ENSP00000321345.5:n.1045+59C>G
ENST00000395227.2:c.-59+17131C>G	ENSP00000378652.2:n.-59+17131C>G
ENST00000425614.3:c.280+59C>G	ENSP00000387640.2:n.280+59C>G
ENST00000473881.2:c.190+17131C>G	ENSP00000486667.1:n.190+17131C>G
NM_144701.2:c.1045+59C>G	NP_653302.2:n.1045+59C>G
XM_005270516.2:c.283+59C>G	XP_005270573.1:n.283+59C>G
XM_011540789.1:c.1135+59C>G	XP_011539091.1:n.1135+59C>G
XM_011540790.1:c.1045+59C>G	XP_011539092.1:n.1045+59C>G
XM_011540791.1:c.1045+59C>G	XP_011539093.1:n.1045+59C>G
XM_011540790.3:c.1045+59C>G	XP_011539092.1:n.1045+59C>G
XM_011540791.3:c.1045+59C>G	XP_011539093.1:n.1045+59C>G
XR_001736993.1:n.1228+59C>G
NM_144701.3:c.1045+59C>G MANE Select	NP_653302.2:n.1045+59C>G