Canonical Allele Identifier: CA2646126140
Gene: IL23R HGNC NCBI

Linked Data

gnomAD v4: 1-67259436-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259436T>C , CM000663.2:g.67259436T>C GRCh38
NC_000001.10:g.67725119T>C , CM000663.1:g.67725119T>C GRCh37
NC_000001.9:g.67497707T>C NCBI36
NG_011498.1:g.97951T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*308T>C MANE Select ENSP00000321345.5:n.*308T>C
ENST00000347310.9:c.*308T>C ENSP00000321345.5:n.*308T>C
ENST00000395227.2:c.*308T>C ENSP00000378652.2:n.*308T>C
ENST00000473881.2:c.*1024T>C ENSP00000486667.1:n.*1024T>C
NM_144701.2:c.*308T>C NP_653302.2:n.*308T>C
XM_005270516.2:c.*308T>C XP_005270573.1:n.*308T>C
XM_011540789.1:c.*308T>C XP_011539091.1:n.*308T>C
XM_011540790.1:c.*308T>C XP_011539092.1:n.*308T>C
XM_011540791.1:c.*308T>C XP_011539093.1:n.*308T>C
XM_011540790.3:c.*308T>C XP_011539092.1:n.*308T>C
XM_011540791.3:c.*308T>C XP_011539093.1:n.*308T>C
NM_144701.3:c.*308T>C MANE Select NP_653302.2:n.*308T>C
Search 100 bp 5'
Search 100 bp 3'