Canonical Allele Identifier: CA2646126203

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259504-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259509del , CM000663.2:g.67259509del	GRCh38
NC_000001.10:g.67725192del , CM000663.1:g.67725192del	GRCh37
NC_000001.9:g.67497780del	NCBI36
NG_011498.1:g.98024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*381del MANE Select	ENSP00000321345.5:n.*381del
ENST00000347310.9:c.*381del	ENSP00000321345.5:n.*381del
ENST00000395227.2:c.*381del	ENSP00000378652.2:n.*381del
ENST00000473881.2:c.*1097del	ENSP00000486667.1:n.*1097del
NM_144701.2:c.*381del	NP_653302.2:n.*381del
XM_005270516.2:c.*381del	XP_005270573.1:n.*381del
XM_011540789.1:c.*381del	XP_011539091.1:n.*381del
XM_011540790.1:c.*381del	XP_011539092.1:n.*381del
XM_011540791.1:c.*381del	XP_011539093.1:n.*381del
XM_011540790.3:c.*381del	XP_011539092.1:n.*381del
XM_011540791.3:c.*381del	XP_011539093.1:n.*381del
NM_144701.3:c.*381del MANE Select	NP_653302.2:n.*381del