Canonical Allele Identifier: CA738095319
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259406T>G , CM000663.2:g.67259406T>G GRCh38
NC_000001.10:g.67725089T>G , CM000663.1:g.67725089T>G GRCh37
NC_000001.9:g.67497677T>G NCBI36
NG_011498.1:g.97921T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*278T>G MANE Select ENSP00000321345.5:n.*278T>G
ENST00000347310.9:c.*278T>G ENSP00000321345.5:n.*278T>G
ENST00000395227.2:c.*278T>G ENSP00000378652.2:n.*278T>G
ENST00000473881.2:c.*994T>G ENSP00000486667.1:n.*994T>G
NM_144701.2:c.*278T>G NP_653302.2:n.*278T>G
XM_005270516.2:c.*278T>G XP_005270573.1:n.*278T>G
XM_011540789.1:c.*278T>G XP_011539091.1:n.*278T>G
XM_011540790.1:c.*278T>G XP_011539092.1:n.*278T>G
XM_011540791.1:c.*278T>G XP_011539093.1:n.*278T>G
XM_011540790.3:c.*278T>G XP_011539092.1:n.*278T>G
XM_011540791.3:c.*278T>G XP_011539093.1:n.*278T>G
NM_144701.3:c.*278T>G MANE Select NP_653302.2:n.*278T>G