Canonical Allele Identifier: CA23506800

Gene: IL23R

Linked Data

• dbSNP Id: rs764164402
• gnomAD v2: 1-67724940-CAT-C
• gnomAD v3: 1-67259257-CAT-C
• gnomAD v4: 1-67259257-CAT-C
• MyVariant Identifiers: chr1:g.67724941_67724942del (hg19) ; chr1:g.67259258_67259259del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259258_67259259del , CM000663.2:g.67259258_67259259del	GRCh38
NC_000001.10:g.67724941_67724942del , CM000663.1:g.67724941_67724942del	GRCh37
NC_000001.9:g.67497529_67497530del	NCBI36
NG_011498.1:g.97773_97774del

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*130_*131del MANE Select	ENSP00000321345.5:n.*130_*131del
ENST00000347310.9:c.*130_*131del	ENSP00000321345.5:n.*130_*131del
ENST00000395227.2:c.*130_*131del	ENSP00000378652.2:n.*130_*131del
ENST00000473881.2:c.*846_*847del	ENSP00000486667.1:n.*846_*847del
NM_144701.2:c.*130_*131del	NP_653302.2:n.*130_*131del
XM_005270516.2:c.*130_*131del	XP_005270573.1:n.*130_*131del
XM_011540789.1:c.*130_*131del	XP_011539091.1:n.*130_*131del
XM_011540790.1:c.*130_*131del	XP_011539092.1:n.*130_*131del
XM_011540791.1:c.*130_*131del	XP_011539093.1:n.*130_*131del
XM_011540790.3:c.*130_*131del	XP_011539092.1:n.*130_*131del
XM_011540791.3:c.*130_*131del	XP_011539093.1:n.*130_*131del
NM_144701.3:c.*130_*131del MANE Select	NP_653302.2:n.*130_*131del