Canonical Allele Identifier: CA340725735

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705864A>T (hg19) ; chr1:g.67240181A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240181A>T , CM000663.2:g.67240181A>T	GRCh38
NC_000001.10:g.67705864A>T , CM000663.1:g.67705864A>T	GRCh37
NC_000001.9:g.67478452A>T	NCBI36
NG_011498.1:g.78696A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.924A>T	ENSP00000513137.1:n.924A>T
ENST00000697149.1:c.887A>T	ENSP00000513138.1:n.887A>T
ENST00000697150.1:c.1045+3379A>T	ENSP00000513139.1:n.1045+3379A>T
ENST00000697151.1:c.1045+3379A>T	ENSP00000513140.1:n.1045+3379A>T
ENST00000697152.1:c.799-15656A>T	ENSP00000513141.1:n.799-15656A>T
ENST00000697153.1:c.795-15656A>T	ENSP00000513142.1:n.795-15656A>T
ENST00000697154.1:c.956-18297A>T	ENSP00000513143.1:n.956-18297A>T
ENST00000697155.1:c.649-18297A>T	ENSP00000513144.1:n.649-18297A>T
ENST00000697156.1:c.1048A>T	ENSP00000513145.1:p.Asn350Tyr
ENST00000697157.1:c.902A>T	ENSP00000513146.1:n.902A>T
ENST00000697158.1:c.891A>T	ENSP00000513147.1:n.891A>T
ENST00000697159.1:c.741A>T	ENSP00000513148.1:n.741A>T
ENST00000697160.1:c.956-15656A>T	ENSP00000513149.1:n.956-15656A>T
ENST00000697161.1:c.584A>T	ENSP00000513150.1:n.584A>T
ENST00000697162.1:c.977A>T	ENSP00000513151.1:n.977A>T
ENST00000697163.1:c.1048A>T	ENSP00000513152.1:p.Asn350Tyr
ENST00000697164.1:c.958A>T	ENSP00000513153.1:p.Asn320Tyr
ENST00000697165.1:c.745A>T	ENSP00000513154.1:p.Asn249Tyr
ENST00000697223.1:c.797A>T	ENSP00000513190.1:n.797A>T
ENST00000697224.1:c.884+3379A>T	ENSP00000513191.1:n.884+3379A>T
ENST00000697225.1:c.651A>T	ENSP00000513192.1:n.651A>T
ENST00000697226.1:c.738+3379A>T	ENSP00000513193.1:n.738+3379A>T
ENST00000697227.1:c.884A>T	ENSP00000513194.1:n.884A>T
ENST00000697228.1:c.740A>T	ENSP00000513195.1:n.740A>T
ENST00000697229.1:c.885-15656A>T	ENSP00000513196.1:n.885-15656A>T
ENST00000697230.1:c.958A>T	ENSP00000513197.1:p.Asn320Tyr
ENST00000697231.1:c.953A>T	ENSP00000513198.1:n.953A>T
ENST00000697232.1:c.977A>T	ENSP00000513199.1:n.977A>T
ENST00000347310.10:c.1048A>T MANE Select	ENSP00000321345.5:p.Asn350Tyr
ENST00000637002.1:c.439A>T	ENSP00000490340.1:p.Asn147Tyr
ENST00000347310.9:c.1048A>T	ENSP00000321345.5:p.Asn350Tyr
ENST00000395227.2:c.-58-15656A>T	ENSP00000378652.2:n.-58-15656A>T
ENST00000425614.3:c.283A>T	ENSP00000387640.2:p.Asn95Tyr
ENST00000473881.2:c.191-15656A>T	ENSP00000486667.1:n.191-15656A>T
NM_144701.2:c.1048A>T	NP_653302.2:p.Asn350Tyr
XM_005270516.2:c.286A>T	XP_005270573.1:p.Asn96Tyr
XM_011540789.1:c.1138A>T	XP_011539091.1:p.Asn380Tyr
XM_011540790.1:c.1048A>T	XP_011539092.1:p.Asn350Tyr
XM_011540791.1:c.1048A>T	XP_011539093.1:p.Asn350Tyr
XM_011540790.3:c.1048A>T	XP_011539092.1:p.Asn350Tyr
XM_011540791.3:c.1048A>T	XP_011539093.1:p.Asn350Tyr
XR_001736993.1:n.1228+3379A>T
NM_144701.3:c.1048A>T MANE Select	NP_653302.2:p.Asn350Tyr