Canonical Allele Identifier: CA738095299
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259367G>C , CM000663.2:g.67259367G>C GRCh38
NC_000001.10:g.67725050G>C , CM000663.1:g.67725050G>C GRCh37
NC_000001.9:g.67497638G>C NCBI36
NG_011498.1:g.97882G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*239G>C MANE Select ENSP00000321345.5:n.*239G>C
ENST00000347310.9:c.*239G>C ENSP00000321345.5:n.*239G>C
ENST00000395227.2:c.*239G>C ENSP00000378652.2:n.*239G>C
ENST00000473881.2:c.*955G>C ENSP00000486667.1:n.*955G>C
NM_144701.2:c.*239G>C NP_653302.2:n.*239G>C
XM_005270516.2:c.*239G>C XP_005270573.1:n.*239G>C
XM_011540789.1:c.*239G>C XP_011539091.1:n.*239G>C
XM_011540790.1:c.*239G>C XP_011539092.1:n.*239G>C
XM_011540791.1:c.*239G>C XP_011539093.1:n.*239G>C
XM_011540790.3:c.*239G>C XP_011539092.1:n.*239G>C
XM_011540791.3:c.*239G>C XP_011539093.1:n.*239G>C
NM_144701.3:c.*239G>C MANE Select NP_653302.2:n.*239G>C