Canonical Allele Identifier: CA2646126145
Gene: IL23R HGNC NCBI

Linked Data

gnomAD v4: 1-67259441-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259442del , CM000663.2:g.67259442del GRCh38
NC_000001.10:g.67725125del , CM000663.1:g.67725125del GRCh37
NC_000001.9:g.67497713del NCBI36
NG_011498.1:g.97957del

Transcript Alleles

HGVS Amino-acid Change
ENST00000347310.10:c.*314del MANE Select ENSP00000321345.5:n.*314del
ENST00000347310.9:c.*314del ENSP00000321345.5:n.*314del
ENST00000395227.2:c.*314del ENSP00000378652.2:n.*314del
ENST00000473881.2:c.*1030del ENSP00000486667.1:n.*1030del
NM_144701.2:c.*314del NP_653302.2:n.*314del
XM_005270516.2:c.*314del XP_005270573.1:n.*314del
XM_011540789.1:c.*314del XP_011539091.1:n.*314del
XM_011540790.1:c.*314del XP_011539092.1:n.*314del
XM_011540791.1:c.*314del XP_011539093.1:n.*314del
XM_011540790.3:c.*314del XP_011539092.1:n.*314del
XM_011540791.3:c.*314del XP_011539093.1:n.*314del
NM_144701.3:c.*314del MANE Select NP_653302.2:n.*314del
Search 100 bp 5'
Search 100 bp 3'