Canonical Allele Identifier: CA1173064463
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259407G= , CM000663.2:g.67259407G= GRCh38
NC_000001.10:g.67725090G= , CM000663.1:g.67725090G= GRCh37
NC_000001.9:g.67497678G= NCBI36
NG_011498.1:g.97922G=

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*279G= MANE Select ENSP00000321345.5:n.*279G=
ENST00000347310.9:c.*279G= ENSP00000321345.5:n.*279G=
ENST00000395227.2:c.*279G= ENSP00000378652.2:n.*279G=
ENST00000473881.2:c.*995G= ENSP00000486667.1:n.*995G=
NM_144701.2:c.*279G= NP_653302.2:n.*279G=
XM_005270516.2:c.*279G= XP_005270573.1:n.*279G=
XM_011540789.1:c.*279G= XP_011539091.1:n.*279G=
XM_011540790.1:c.*279G= XP_011539092.1:n.*279G=
XM_011540791.1:c.*279G= XP_011539093.1:n.*279G=
XM_011540790.3:c.*279G= XP_011539092.1:n.*279G=
XM_011540791.3:c.*279G= XP_011539093.1:n.*279G=
NM_144701.3:c.*279G= MANE Select NP_653302.2:n.*279G=