Canonical Allele Identifier: CA738070294

Gene: IL23R

Linked Data

• dbSNP Id: rs1312995836
• gnomAD v3: 1-67240132-A-G
• gnomAD v4: 1-67240132-A-G
• MyVariant Identifiers: chr1:g.67705815A>G (hg19) ; chr1:g.67240132A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240132A>G , CM000663.2:g.67240132A>G	GRCh38
NC_000001.10:g.67705815A>G , CM000663.1:g.67705815A>G	GRCh37
NC_000001.9:g.67478403A>G	NCBI36
NG_011498.1:g.78647A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.922-47A>G	ENSP00000513137.1:n.922-47A>G
ENST00000697149.1:c.885-47A>G	ENSP00000513138.1:n.885-47A>G
ENST00000697150.1:c.1045+3330A>G	ENSP00000513139.1:n.1045+3330A>G
ENST00000697151.1:c.1045+3330A>G	ENSP00000513140.1:n.1045+3330A>G
ENST00000697152.1:c.799-15705A>G	ENSP00000513141.1:n.799-15705A>G
ENST00000697153.1:c.795-15705A>G	ENSP00000513142.1:n.795-15705A>G
ENST00000697154.1:c.956-18346A>G	ENSP00000513143.1:n.956-18346A>G
ENST00000697155.1:c.649-18346A>G	ENSP00000513144.1:n.649-18346A>G
ENST00000697156.1:c.1046-47A>G	ENSP00000513145.1:n.1046-47A>G
ENST00000697157.1:c.900-47A>G	ENSP00000513146.1:n.900-47A>G
ENST00000697158.1:c.889-47A>G	ENSP00000513147.1:n.889-47A>G
ENST00000697159.1:c.739-47A>G	ENSP00000513148.1:n.739-47A>G
ENST00000697160.1:c.956-15705A>G	ENSP00000513149.1:n.956-15705A>G
ENST00000697161.1:c.582-47A>G	ENSP00000513150.1:n.582-47A>G
ENST00000697162.1:c.975-47A>G	ENSP00000513151.1:n.975-47A>G
ENST00000697163.1:c.1046-47A>G	ENSP00000513152.1:n.1046-47A>G
ENST00000697164.1:c.956-47A>G	ENSP00000513153.1:n.956-47A>G
ENST00000697165.1:c.743-47A>G	ENSP00000513154.1:n.743-47A>G
ENST00000697223.1:c.795-47A>G	ENSP00000513190.1:n.795-47A>G
ENST00000697224.1:c.884+3330A>G	ENSP00000513191.1:n.884+3330A>G
ENST00000697225.1:c.649-47A>G	ENSP00000513192.1:n.649-47A>G
ENST00000697226.1:c.738+3330A>G	ENSP00000513193.1:n.738+3330A>G
ENST00000697227.1:c.882-47A>G	ENSP00000513194.1:n.882-47A>G
ENST00000697228.1:c.738-47A>G	ENSP00000513195.1:n.738-47A>G
ENST00000697229.1:c.885-15705A>G	ENSP00000513196.1:n.885-15705A>G
ENST00000697230.1:c.956-47A>G	ENSP00000513197.1:n.956-47A>G
ENST00000697231.1:c.951-47A>G	ENSP00000513198.1:n.951-47A>G
ENST00000697232.1:c.975-47A>G	ENSP00000513199.1:n.975-47A>G
ENST00000347310.10:c.1046-47A>G MANE Select	ENSP00000321345.5:n.1046-47A>G
ENST00000637002.1:c.437-47A>G	ENSP00000490340.1:n.437-47A>G
ENST00000347310.9:c.1046-47A>G	ENSP00000321345.5:n.1046-47A>G
ENST00000395227.2:c.-58-15705A>G	ENSP00000378652.2:n.-58-15705A>G
ENST00000425614.3:c.281-47A>G	ENSP00000387640.2:n.281-47A>G
ENST00000473881.2:c.191-15705A>G	ENSP00000486667.1:n.191-15705A>G
NM_144701.2:c.1046-47A>G	NP_653302.2:n.1046-47A>G
XM_005270516.2:c.284-47A>G	XP_005270573.1:n.284-47A>G
XM_011540789.1:c.1136-47A>G	XP_011539091.1:n.1136-47A>G
XM_011540790.1:c.1046-47A>G	XP_011539092.1:n.1046-47A>G
XM_011540791.1:c.1046-47A>G	XP_011539093.1:n.1046-47A>G
XM_011540790.3:c.1046-47A>G	XP_011539092.1:n.1046-47A>G
XM_011540791.3:c.1046-47A>G	XP_011539093.1:n.1046-47A>G
XR_001736993.1:n.1228+3330A>G
NM_144701.3:c.1046-47A>G MANE Select	NP_653302.2:n.1046-47A>G