Canonical Allele Identifier: CA23506924
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs1020369820

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259399A>G , CM000663.2:g.67259399A>G GRCh38
NC_000001.10:g.67725082A>G , CM000663.1:g.67725082A>G GRCh37
NC_000001.9:g.67497670A>G NCBI36
NG_011498.1:g.97914A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*271A>G MANE Select ENSP00000321345.5:n.*271A>G
ENST00000347310.9:c.*271A>G ENSP00000321345.5:n.*271A>G
ENST00000395227.2:c.*271A>G ENSP00000378652.2:n.*271A>G
ENST00000473881.2:c.*987A>G ENSP00000486667.1:n.*987A>G
NM_144701.2:c.*271A>G NP_653302.2:n.*271A>G
XM_005270516.2:c.*271A>G XP_005270573.1:n.*271A>G
XM_011540789.1:c.*271A>G XP_011539091.1:n.*271A>G
XM_011540790.1:c.*271A>G XP_011539092.1:n.*271A>G
XM_011540791.1:c.*271A>G XP_011539093.1:n.*271A>G
XM_011540790.3:c.*271A>G XP_011539092.1:n.*271A>G
XM_011540791.3:c.*271A>G XP_011539093.1:n.*271A>G
NM_144701.3:c.*271A>G MANE Select NP_653302.2:n.*271A>G