Canonical Allele Identifier: CA340729574

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259012-G-A
• MyVariant Identifiers: chr1:g.67724695G>A (hg19) ; chr1:g.67259012G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259012G>A , CM000663.2:g.67259012G>A	GRCh38
NC_000001.10:g.67724695G>A , CM000663.1:g.67724695G>A	GRCh37
NC_000001.9:g.67497283G>A	NCBI36
NG_011498.1:g.97527G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1613G>A	ENSP00000513138.1:n.1613G>A
ENST00000697150.1:c.1671G>A	ENSP00000513139.1:n.1671G>A
ENST00000697151.1:c.1604G>A	ENSP00000513140.1:n.1604G>A
ENST00000697164.1:c.1684G>A	ENSP00000513153.1:p.Asp562Asn
ENST00000697165.1:c.1471G>A	ENSP00000513154.1:p.Asp491Asn
ENST00000347310.10:c.1774G>A MANE Select	ENSP00000321345.5:p.Asp592Asn
ENST00000637002.1:c.1165G>A	ENSP00000490340.1:p.Asp389Asn
ENST00000347310.9:c.1774G>A	ENSP00000321345.5:p.Asp592Asn
ENST00000395227.2:c.568G>A	ENSP00000378652.2:p.Asp190Asn
ENST00000425614.3:c.1009G>A	ENSP00000387640.2:p.Asp337Asn
ENST00000473881.2:c.*600G>A	ENSP00000486667.1:n.*600G>A
NM_144701.2:c.1774G>A	NP_653302.2:p.Asp592Asn
XM_005270516.2:c.1012G>A	XP_005270573.1:p.Asp338Asn
XM_011540789.1:c.1864G>A	XP_011539091.1:p.Asp622Asn
XM_011540790.1:c.1774G>A	XP_011539092.1:p.Asp592Asn
XM_011540791.1:c.1774G>A	XP_011539093.1:p.Asp592Asn
XM_011540790.3:c.1774G>A	XP_011539092.1:p.Asp592Asn
XM_011540791.3:c.1774G>A	XP_011539093.1:p.Asp592Asn
XR_001736993.1:n.1854G>A
NM_144701.3:c.1774G>A MANE Select	NP_653302.2:p.Asp592Asn