Canonical Allele Identifier: CA23506931
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs965631959

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259401C>T , CM000663.2:g.67259401C>T GRCh38
NC_000001.10:g.67725084C>T , CM000663.1:g.67725084C>T GRCh37
NC_000001.9:g.67497672C>T NCBI36
NG_011498.1:g.97916C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*273C>T MANE Select ENSP00000321345.5:n.*273C>T
ENST00000347310.9:c.*273C>T ENSP00000321345.5:n.*273C>T
ENST00000395227.2:c.*273C>T ENSP00000378652.2:n.*273C>T
ENST00000473881.2:c.*989C>T ENSP00000486667.1:n.*989C>T
NM_144701.2:c.*273C>T NP_653302.2:n.*273C>T
XM_005270516.2:c.*273C>T XP_005270573.1:n.*273C>T
XM_011540789.1:c.*273C>T XP_011539091.1:n.*273C>T
XM_011540790.1:c.*273C>T XP_011539092.1:n.*273C>T
XM_011540791.1:c.*273C>T XP_011539093.1:n.*273C>T
XM_011540790.3:c.*273C>T XP_011539092.1:n.*273C>T
XM_011540791.3:c.*273C>T XP_011539093.1:n.*273C>T
NM_144701.3:c.*273C>T MANE Select NP_653302.2:n.*273C>T