Canonical Allele Identifier: CA1173064425

Gene: IL23R

Linked Data

• dbSNP Id: rs1653116735

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259310_67259325del , CM000663.2:g.67259310_67259325del	GRCh38
NC_000001.10:g.67724993_67725008del , CM000663.1:g.67724993_67725008del	GRCh37
NC_000001.9:g.67497581_67497596del	NCBI36
NG_011498.1:g.97825_97840del

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*182_*197del MANE Select	ENSP00000321345.5:n.*182_*197del
ENST00000347310.9:c.*182_*197del	ENSP00000321345.5:n.*182_*197del
ENST00000395227.2:c.*182_*197del	ENSP00000378652.2:n.*182_*197del
ENST00000473881.2:c.*898_*913del	ENSP00000486667.1:n.*898_*913del
NM_144701.2:c.*182_*197del	NP_653302.2:n.*182_*197del
XM_005270516.2:c.*182_*197del	XP_005270573.1:n.*182_*197del
XM_011540789.1:c.*182_*197del	XP_011539091.1:n.*182_*197del
XM_011540790.1:c.*182_*197del	XP_011539092.1:n.*182_*197del
XM_011540791.1:c.*182_*197del	XP_011539093.1:n.*182_*197del
XM_011540790.3:c.*182_*197del	XP_011539092.1:n.*182_*197del
XM_011540791.3:c.*182_*197del	XP_011539093.1:n.*182_*197del
NM_144701.3:c.*182_*197del MANE Select	NP_653302.2:n.*182_*197del