Canonical Allele Identifier: CA1002754276

Gene: IL23R

Linked Data

• dbSNP Id: rs1653116644
• gnomAD v3: 1-67259309-ATG-A
• gnomAD v4: 1-67259309-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259310_67259311del , CM000663.2:g.67259310_67259311del	GRCh38
NC_000001.10:g.67724993_67724994del , CM000663.1:g.67724993_67724994del	GRCh37
NC_000001.9:g.67497581_67497582del	NCBI36
NG_011498.1:g.97825_97826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*182_*183del MANE Select	ENSP00000321345.5:n.*182_*183del
ENST00000347310.9:c.*182_*183del	ENSP00000321345.5:n.*182_*183del
ENST00000395227.2:c.*182_*183del	ENSP00000378652.2:n.*182_*183del
ENST00000473881.2:c.*898_*899del	ENSP00000486667.1:n.*898_*899del
NM_144701.2:c.*182_*183del	NP_653302.2:n.*182_*183del
XM_005270516.2:c.*182_*183del	XP_005270573.1:n.*182_*183del
XM_011540789.1:c.*182_*183del	XP_011539091.1:n.*182_*183del
XM_011540790.1:c.*182_*183del	XP_011539092.1:n.*182_*183del
XM_011540791.1:c.*182_*183del	XP_011539093.1:n.*182_*183del
XM_011540790.3:c.*182_*183del	XP_011539092.1:n.*182_*183del
XM_011540791.3:c.*182_*183del	XP_011539093.1:n.*182_*183del
NM_144701.3:c.*182_*183del MANE Select	NP_653302.2:n.*182_*183del