Canonical Allele Identifier: CA23506850
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs1055452614

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259342G>T , CM000663.2:g.67259342G>T GRCh38
NC_000001.10:g.67725025G>T , CM000663.1:g.67725025G>T GRCh37
NC_000001.9:g.67497613G>T NCBI36
NG_011498.1:g.97857G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*214G>T MANE Select ENSP00000321345.5:n.*214G>T
ENST00000347310.9:c.*214G>T ENSP00000321345.5:n.*214G>T
ENST00000395227.2:c.*214G>T ENSP00000378652.2:n.*214G>T
ENST00000473881.2:c.*930G>T ENSP00000486667.1:n.*930G>T
NM_144701.2:c.*214G>T NP_653302.2:n.*214G>T
XM_005270516.2:c.*214G>T XP_005270573.1:n.*214G>T
XM_011540789.1:c.*214G>T XP_011539091.1:n.*214G>T
XM_011540790.1:c.*214G>T XP_011539092.1:n.*214G>T
XM_011540791.1:c.*214G>T XP_011539093.1:n.*214G>T
XM_011540790.3:c.*214G>T XP_011539092.1:n.*214G>T
XM_011540791.3:c.*214G>T XP_011539093.1:n.*214G>T
NM_144701.3:c.*214G>T MANE Select NP_653302.2:n.*214G>T