Canonical Allele Identifier: CA340729657

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259033-G-C
• MyVariant Identifiers: chr1:g.67724716G>C (hg19) ; chr1:g.67259033G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259033G>C , CM000663.2:g.67259033G>C	GRCh38
NC_000001.10:g.67724716G>C , CM000663.1:g.67724716G>C	GRCh37
NC_000001.9:g.67497304G>C	NCBI36
NG_011498.1:g.97548G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1634G>C	ENSP00000513138.1:n.1634G>C
ENST00000697150.1:c.1692G>C	ENSP00000513139.1:n.1692G>C
ENST00000697151.1:c.1625G>C	ENSP00000513140.1:n.1625G>C
ENST00000697164.1:c.1705G>C	ENSP00000513153.1:p.Gly569Arg
ENST00000697165.1:c.1492G>C	ENSP00000513154.1:p.Gly498Arg
ENST00000347310.10:c.1795G>C MANE Select	ENSP00000321345.5:p.Gly599Arg
ENST00000637002.1:c.1186G>C	ENSP00000490340.1:p.Gly396Arg
ENST00000347310.9:c.1795G>C	ENSP00000321345.5:p.Gly599Arg
ENST00000395227.2:c.589G>C	ENSP00000378652.2:p.Gly197Arg
ENST00000425614.3:c.1030G>C	ENSP00000387640.2:p.Gly344Arg
ENST00000473881.2:c.*621G>C	ENSP00000486667.1:n.*621G>C
NM_144701.2:c.1795G>C	NP_653302.2:p.Gly599Arg
XM_005270516.2:c.1033G>C	XP_005270573.1:p.Gly345Arg
XM_011540789.1:c.1885G>C	XP_011539091.1:p.Gly629Arg
XM_011540790.1:c.1795G>C	XP_011539092.1:p.Gly599Arg
XM_011540791.1:c.1795G>C	XP_011539093.1:p.Gly599Arg
XM_011540790.3:c.1795G>C	XP_011539092.1:p.Gly599Arg
XM_011540791.3:c.1795G>C	XP_011539093.1:p.Gly599Arg
XR_001736993.1:n.1875G>C
NM_144701.3:c.1795G>C MANE Select	NP_653302.2:p.Gly599Arg