Canonical Allele Identifier: CA738095399

Gene: IL23R

Linked Data

• dbSNP Id: rs1249633536
• gnomAD v3: 1-67259580-AGAT-A
• gnomAD v4: 1-67259580-AGAT-A
• MyVariant Identifiers: chr1:g.67725264_67725266del (hg19) ; chr1:g.67259581_67259583del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259582_67259584del , CM000663.2:g.67259582_67259584del	GRCh38
NC_000001.10:g.67725265_67725267del , CM000663.1:g.67725265_67725267del	GRCh37
NC_000001.9:g.67497853_67497855del	NCBI36
NG_011498.1:g.98097_98099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*454_*456del MANE Select	ENSP00000321345.5:n.*454_*456del
ENST00000347310.9:c.*454_*456del	ENSP00000321345.5:n.*454_*456del
ENST00000395227.2:c.*454_*456del	ENSP00000378652.2:n.*454_*456del
ENST00000473881.2:c.*1170_*1172del	ENSP00000486667.1:n.*1170_*1172del
NM_144701.2:c.*454_*456del	NP_653302.2:n.*454_*456del
XM_005270516.2:c.*454_*456del	XP_005270573.1:n.*454_*456del
XM_011540789.1:c.*454_*456del	XP_011539091.1:n.*454_*456del
XM_011540790.1:c.*454_*456del	XP_011539092.1:n.*454_*456del
XM_011540791.1:c.*454_*456del	XP_011539093.1:n.*454_*456del
XM_011540790.3:c.*454_*456del	XP_011539092.1:n.*454_*456del
XM_011540791.3:c.*454_*456del	XP_011539093.1:n.*454_*456del
NM_144701.3:c.*454_*456del MANE Select	NP_653302.2:n.*454_*456del