Canonical Allele Identifier: CA1173064432

Gene: IL23R

Linked Data

• dbSNP Id: rs1653117350
• gnomAD v4: 1-67259317-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259320_67259321del , CM000663.2:g.67259320_67259321del	GRCh38
NC_000001.10:g.67725003_67725004del , CM000663.1:g.67725003_67725004del	GRCh37
NC_000001.9:g.67497591_67497592del	NCBI36
NG_011498.1:g.97835_97836del

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*192_*193del MANE Select	ENSP00000321345.5:n.*192_*193del
ENST00000347310.9:c.*192_*193del	ENSP00000321345.5:n.*192_*193del
ENST00000395227.2:c.*192_*193del	ENSP00000378652.2:n.*192_*193del
ENST00000473881.2:c.*908_*909del	ENSP00000486667.1:n.*908_*909del
NM_144701.2:c.*192_*193del	NP_653302.2:n.*192_*193del
XM_005270516.2:c.*192_*193del	XP_005270573.1:n.*192_*193del
XM_011540789.1:c.*192_*193del	XP_011539091.1:n.*192_*193del
XM_011540790.1:c.*192_*193del	XP_011539092.1:n.*192_*193del
XM_011540791.1:c.*192_*193del	XP_011539093.1:n.*192_*193del
XM_011540790.3:c.*192_*193del	XP_011539092.1:n.*192_*193del
XM_011540791.3:c.*192_*193del	XP_011539093.1:n.*192_*193del
NM_144701.3:c.*192_*193del MANE Select	NP_653302.2:n.*192_*193del