Canonical Allele Identifier: CA523607598

Gene: IL23R

Linked Data

• dbSNP Id: rs1410897554
• gnomAD v2: 1-67724890-CTGCCTCTTTT-C
• gnomAD v4: 1-67259207-CTGCCTCTTTT-C
• MyVariant Identifiers: chr1:g.67724891_67724900del (hg19) ; chr1:g.67259208_67259217del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259210_67259219del , CM000663.2:g.67259210_67259219del	GRCh38
NC_000001.10:g.67724893_67724902del , CM000663.1:g.67724893_67724902del	GRCh37
NC_000001.9:g.67497481_67497490del	NCBI36
NG_011498.1:g.97725_97734del

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*82_*91del MANE Select	ENSP00000321345.5:n.*82_*91del
ENST00000347310.9:c.*82_*91del	ENSP00000321345.5:n.*82_*91del
ENST00000395227.2:c.*82_*91del	ENSP00000378652.2:n.*82_*91del
ENST00000425614.3:c.*82_*91del	ENSP00000387640.2:n.*82_*91del
ENST00000473881.2:c.*798_*807del	ENSP00000486667.1:n.*798_*807del
NM_144701.2:c.*82_*91del	NP_653302.2:n.*82_*91del
XM_005270516.2:c.*82_*91del	XP_005270573.1:n.*82_*91del
XM_011540789.1:c.*82_*91del	XP_011539091.1:n.*82_*91del
XM_011540790.1:c.*82_*91del	XP_011539092.1:n.*82_*91del
XM_011540791.1:c.*82_*91del	XP_011539093.1:n.*82_*91del
XM_011540790.3:c.*82_*91del	XP_011539092.1:n.*82_*91del
XM_011540791.3:c.*82_*91del	XP_011539093.1:n.*82_*91del
NM_144701.3:c.*82_*91del MANE Select	NP_653302.2:n.*82_*91del