Canonical Allele Identifier: CA23506915
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs552507254

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259396G>A , CM000663.2:g.67259396G>A GRCh38
NC_000001.10:g.67725079G>A , CM000663.1:g.67725079G>A GRCh37
NC_000001.9:g.67497667G>A NCBI36
NG_011498.1:g.97911G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*268G>A MANE Select ENSP00000321345.5:n.*268G>A
ENST00000347310.9:c.*268G>A ENSP00000321345.5:n.*268G>A
ENST00000395227.2:c.*268G>A ENSP00000378652.2:n.*268G>A
ENST00000473881.2:c.*984G>A ENSP00000486667.1:n.*984G>A
NM_144701.2:c.*268G>A NP_653302.2:n.*268G>A
XM_005270516.2:c.*268G>A XP_005270573.1:n.*268G>A
XM_011540789.1:c.*268G>A XP_011539091.1:n.*268G>A
XM_011540790.1:c.*268G>A XP_011539092.1:n.*268G>A
XM_011540791.1:c.*268G>A XP_011539093.1:n.*268G>A
XM_011540790.3:c.*268G>A XP_011539092.1:n.*268G>A
XM_011540791.3:c.*268G>A XP_011539093.1:n.*268G>A
NM_144701.3:c.*268G>A MANE Select NP_653302.2:n.*268G>A