Canonical Allele Identifier: CA738092684

Gene: IL23R

Linked Data

• dbSNP Id: rs910190194
• MyVariant Identifiers: chr1:g.67721131_67721132del (hg19) ; chr1:g.67255448_67255449del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67255456_67255457del , CM000663.2:g.67255456_67255457del	GRCh38
NC_000001.10:g.67721139_67721140del , CM000663.1:g.67721139_67721140del	GRCh37
NC_000001.9:g.67493727_67493728del	NCBI36
NG_011498.1:g.93971_93972del

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.1025-381_1025-380del	ENSP00000513137.1:n.1025-381_1025-380del
ENST00000697149.1:c.988-381_988-380del	ENSP00000513138.1:n.988-381_988-380del
ENST00000697150.1:c.1046-381_1046-380del	ENSP00000513139.1:n.1046-381_1046-380del
ENST00000697151.1:c.1046-381_1046-380del	ENSP00000513140.1:n.1046-381_1046-380del
ENST00000697152.1:c.799-381_799-380del	ENSP00000513141.1:n.799-381_799-380del
ENST00000697153.1:c.795-381_795-380del	ENSP00000513142.1:n.795-381_795-380del
ENST00000697154.1:c.956-3022_956-3021del	ENSP00000513143.1:n.956-3022_956-3021del
ENST00000697155.1:c.649-3022_649-3021del	ENSP00000513144.1:n.649-3022_649-3021del
ENST00000697156.1:c.1282-381_1282-380del	ENSP00000513145.1:n.1282-381_1282-380del
ENST00000697157.1:c.1003-381_1003-380del	ENSP00000513146.1:n.1003-381_1003-380del
ENST00000697158.1:c.992-381_992-380del	ENSP00000513147.1:n.992-381_992-380del
ENST00000697159.1:c.842-381_842-380del	ENSP00000513148.1:n.842-381_842-380del
ENST00000697160.1:c.956-381_956-380del	ENSP00000513149.1:n.956-381_956-380del
ENST00000697161.1:c.685-381_685-380del	ENSP00000513150.1:n.685-381_685-380del
ENST00000697162.1:c.1078-381_1078-380del	ENSP00000513151.1:n.1078-381_1078-380del
ENST00000697163.1:c.1149-381_1149-380del	ENSP00000513152.1:n.1149-381_1149-380del
ENST00000697164.1:c.1059-381_1059-380del	ENSP00000513153.1:n.1059-381_1059-380del
ENST00000697165.1:c.846-381_846-380del	ENSP00000513154.1:n.846-381_846-380del
ENST00000697223.1:c.898-381_898-380del	ENSP00000513190.1:n.898-381_898-380del
ENST00000697224.1:c.885-381_885-380del	ENSP00000513191.1:n.885-381_885-380del
ENST00000697225.1:c.752-381_752-380del	ENSP00000513192.1:n.752-381_752-380del
ENST00000697226.1:c.739-381_739-380del	ENSP00000513193.1:n.739-381_739-380del
ENST00000697227.1:c.985-381_985-380del	ENSP00000513194.1:n.985-381_985-380del
ENST00000697228.1:c.841-381_841-380del	ENSP00000513195.1:n.841-381_841-380del
ENST00000697229.1:c.885-381_885-380del	ENSP00000513196.1:n.885-381_885-380del
ENST00000697230.1:c.1059-381_1059-380del	ENSP00000513197.1:n.1059-381_1059-380del
ENST00000697231.1:c.1054-381_1054-380del	ENSP00000513198.1:n.1054-381_1054-380del
ENST00000697232.1:c.1240-381_1240-380del	ENSP00000513199.1:n.1240-381_1240-380del
ENST00000347310.10:c.1149-381_1149-380del MANE Select	ENSP00000321345.5:n.1149-381_1149-380del
ENST00000637002.1:c.540-381_540-380del	ENSP00000490340.1:n.540-381_540-380del
ENST00000347310.9:c.1149-381_1149-380del	ENSP00000321345.5:n.1149-381_1149-380del
ENST00000395227.2:c.-58-381_-58-380del	ENSP00000378652.2:n.-58-381_-58-380del
ENST00000425614.3:c.384-381_384-380del	ENSP00000387640.2:n.384-381_384-380del
ENST00000473881.2:c.191-381_191-380del	ENSP00000486667.1:n.191-381_191-380del
NM_144701.2:c.1149-381_1149-380del	NP_653302.2:n.1149-381_1149-380del
XM_005270516.2:c.387-381_387-380del	XP_005270573.1:n.387-381_387-380del
XM_011540789.1:c.1239-381_1239-380del	XP_011539091.1:n.1239-381_1239-380del
XM_011540790.1:c.1149-381_1149-380del	XP_011539092.1:n.1149-381_1149-380del
XM_011540791.1:c.1149-381_1149-380del	XP_011539093.1:n.1149-381_1149-380del
XM_011540790.3:c.1149-381_1149-380del	XP_011539092.1:n.1149-381_1149-380del
XM_011540791.3:c.1149-381_1149-380del	XP_011539093.1:n.1149-381_1149-380del
XR_001736993.1:n.1229-381_1229-380del
NM_144701.3:c.1149-381_1149-380del MANE Select	NP_653302.2:n.1149-381_1149-380del