Canonical Allele Identifier: CA738095351
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs1489672358
gnomAD v3: 1-67259467-G-A
gnomAD v4: 1-67259467-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259467G>A , CM000663.2:g.67259467G>A GRCh38
NC_000001.10:g.67725150G>A , CM000663.1:g.67725150G>A GRCh37
NC_000001.9:g.67497738G>A NCBI36
NG_011498.1:g.97982G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*339G>A MANE Select ENSP00000321345.5:n.*339G>A
ENST00000347310.9:c.*339G>A ENSP00000321345.5:n.*339G>A
ENST00000395227.2:c.*339G>A ENSP00000378652.2:n.*339G>A
ENST00000473881.2:c.*1055G>A ENSP00000486667.1:n.*1055G>A
NM_144701.2:c.*339G>A NP_653302.2:n.*339G>A
XM_005270516.2:c.*339G>A XP_005270573.1:n.*339G>A
XM_011540789.1:c.*339G>A XP_011539091.1:n.*339G>A
XM_011540790.1:c.*339G>A XP_011539092.1:n.*339G>A
XM_011540791.1:c.*339G>A XP_011539093.1:n.*339G>A
XM_011540790.3:c.*339G>A XP_011539092.1:n.*339G>A
XM_011540791.3:c.*339G>A XP_011539093.1:n.*339G>A
NM_144701.3:c.*339G>A MANE Select NP_653302.2:n.*339G>A