Canonical Allele Identifier: CA2646125936
Gene: IL23R HGNC NCBI

Linked Data

gnomAD v4: 1-67259156-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259156A>C , CM000663.2:g.67259156A>C GRCh38
NC_000001.10:g.67724839A>C , CM000663.1:g.67724839A>C GRCh37
NC_000001.9:g.67497427A>C NCBI36
NG_011498.1:g.97671A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*28A>C MANE Select ENSP00000321345.5:n.*28A>C
ENST00000637002.1:c.*28A>C ENSP00000490340.1:n.*28A>C
ENST00000347310.9:c.*28A>C ENSP00000321345.5:n.*28A>C
ENST00000395227.2:c.*28A>C ENSP00000378652.2:n.*28A>C
ENST00000425614.3:c.*28A>C ENSP00000387640.2:n.*28A>C
ENST00000473881.2:c.*744A>C ENSP00000486667.1:n.*744A>C
NM_144701.2:c.*28A>C NP_653302.2:n.*28A>C
XM_005270516.2:c.*28A>C XP_005270573.1:n.*28A>C
XM_011540789.1:c.*28A>C XP_011539091.1:n.*28A>C
XM_011540790.1:c.*28A>C XP_011539092.1:n.*28A>C
XM_011540791.1:c.*28A>C XP_011539093.1:n.*28A>C
XM_011540790.3:c.*28A>C XP_011539092.1:n.*28A>C
XM_011540791.3:c.*28A>C XP_011539093.1:n.*28A>C
NM_144701.3:c.*28A>C MANE Select NP_653302.2:n.*28A>C
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