Canonical Allele Identifier: CA523282926
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs954564885
gnomAD v2: 1-67725132-T-A
gnomAD v3: 1-67259449-T-A
gnomAD v4: 1-67259449-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259449T>A , CM000663.2:g.67259449T>A GRCh38
NC_000001.10:g.67725132T>A , CM000663.1:g.67725132T>A GRCh37
NC_000001.9:g.67497720T>A NCBI36
NG_011498.1:g.97964T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*321T>A MANE Select ENSP00000321345.5:n.*321T>A
ENST00000347310.9:c.*321T>A ENSP00000321345.5:n.*321T>A
ENST00000395227.2:c.*321T>A ENSP00000378652.2:n.*321T>A
ENST00000473881.2:c.*1037T>A ENSP00000486667.1:n.*1037T>A
NM_144701.2:c.*321T>A NP_653302.2:n.*321T>A
XM_005270516.2:c.*321T>A XP_005270573.1:n.*321T>A
XM_011540789.1:c.*321T>A XP_011539091.1:n.*321T>A
XM_011540790.1:c.*321T>A XP_011539092.1:n.*321T>A
XM_011540791.1:c.*321T>A XP_011539093.1:n.*321T>A
XM_011540790.3:c.*321T>A XP_011539092.1:n.*321T>A
XM_011540791.3:c.*321T>A XP_011539093.1:n.*321T>A
NM_144701.3:c.*321T>A MANE Select NP_653302.2:n.*321T>A