Canonical Allele Identifier: CA738095287

Gene: IL23R

Linked Data

• dbSNP Id: rs1447419172
• gnomAD v4: 1-67259296-A-G
• MyVariant Identifiers: chr1:g.67724979A>G (hg19) ; chr1:g.67259296A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259296A>G , CM000663.2:g.67259296A>G	GRCh38
NC_000001.10:g.67724979A>G , CM000663.1:g.67724979A>G	GRCh37
NC_000001.9:g.67497567A>G	NCBI36
NG_011498.1:g.97811A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*168A>G MANE Select	ENSP00000321345.5:n.*168A>G
ENST00000347310.9:c.*168A>G	ENSP00000321345.5:n.*168A>G
ENST00000395227.2:c.*168A>G	ENSP00000378652.2:n.*168A>G
ENST00000473881.2:c.*884A>G	ENSP00000486667.1:n.*884A>G
NM_144701.2:c.*168A>G	NP_653302.2:n.*168A>G
XM_005270516.2:c.*168A>G	XP_005270573.1:n.*168A>G
XM_011540789.1:c.*168A>G	XP_011539091.1:n.*168A>G
XM_011540790.1:c.*168A>G	XP_011539092.1:n.*168A>G
XM_011540791.1:c.*168A>G	XP_011539093.1:n.*168A>G
XM_011540790.3:c.*168A>G	XP_011539092.1:n.*168A>G
XM_011540791.3:c.*168A>G	XP_011539093.1:n.*168A>G
NM_144701.3:c.*168A>G MANE Select	NP_653302.2:n.*168A>G