Canonical Allele Identifier: CA2580576877
Gene: IL23R HGNC NCBI

Linked Data

gnomAD v4: 1-67259437-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259437C>G , CM000663.2:g.67259437C>G GRCh38
NC_000001.10:g.67725120C>G , CM000663.1:g.67725120C>G GRCh37
NC_000001.9:g.67497708C>G NCBI36
NG_011498.1:g.97952C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*309C>G MANE Select ENSP00000321345.5:n.*309C>G
ENST00000347310.9:c.*309C>G ENSP00000321345.5:n.*309C>G
ENST00000395227.2:c.*309C>G ENSP00000378652.2:n.*309C>G
ENST00000473881.2:c.*1025C>G ENSP00000486667.1:n.*1025C>G
NM_144701.2:c.*309C>G NP_653302.2:n.*309C>G
XM_005270516.2:c.*309C>G XP_005270573.1:n.*309C>G
XM_011540789.1:c.*309C>G XP_011539091.1:n.*309C>G
XM_011540790.1:c.*309C>G XP_011539092.1:n.*309C>G
XM_011540791.1:c.*309C>G XP_011539093.1:n.*309C>G
XM_011540790.3:c.*309C>G XP_011539092.1:n.*309C>G
XM_011540791.3:c.*309C>G XP_011539093.1:n.*309C>G
NM_144701.3:c.*309C>G MANE Select NP_653302.2:n.*309C>G