Canonical Allele Identifier: CA738095403

Gene: IL23R

Linked Data

• dbSNP Id: rs1282853649
• gnomAD v3: 1-67259589-ACAGCT-A
• gnomAD v4: 1-67259589-ACAGCT-A
• MyVariant Identifiers: chr1:g.67725273_67725277del (hg19) ; chr1:g.67259590_67259594del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259591_67259595del , CM000663.2:g.67259591_67259595del	GRCh38
NC_000001.10:g.67725274_67725278del , CM000663.1:g.67725274_67725278del	GRCh37
NC_000001.9:g.67497862_67497866del	NCBI36
NG_011498.1:g.98106_98110del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*463_*467del MANE Select	ENSP00000321345.5:n.*463_*467del
ENST00000347310.9:c.*463_*467del	ENSP00000321345.5:n.*463_*467del
ENST00000395227.2:c.*463_*467del	ENSP00000378652.2:n.*463_*467del
ENST00000473881.2:c.*1179_*1183del	ENSP00000486667.1:n.*1179_*1183del
NM_144701.2:c.*463_*467del	NP_653302.2:n.*463_*467del
XM_005270516.2:c.*463_*467del	XP_005270573.1:n.*463_*467del
XM_011540789.1:c.*463_*467del	XP_011539091.1:n.*463_*467del
XM_011540790.1:c.*463_*467del	XP_011539092.1:n.*463_*467del
XM_011540791.1:c.*463_*467del	XP_011539093.1:n.*463_*467del
XM_011540790.3:c.*463_*467del	XP_011539092.1:n.*463_*467del
XM_011540791.3:c.*463_*467del	XP_011539093.1:n.*463_*467del
NM_144701.3:c.*463_*467del MANE Select	NP_653302.2:n.*463_*467del