Canonical Allele Identifier: CA340728761

Gene: IL23R

Linked Data

• dbSNP Id: rs751326080
• gnomAD v2: 1-67724499-G-T
• gnomAD v4: 1-67258816-G-T
• MyVariant Identifiers: chr1:g.67724499G>T (hg19) ; chr1:g.67258816G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258816G>T , CM000663.2:g.67258816G>T	GRCh38
NC_000001.10:g.67724499G>T , CM000663.1:g.67724499G>T	GRCh37
NC_000001.9:g.67497087G>T	NCBI36
NG_011498.1:g.97331G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1417G>T	ENSP00000513138.1:n.1417G>T
ENST00000697150.1:c.1475G>T	ENSP00000513139.1:n.1475G>T
ENST00000697151.1:c.1408G>T	ENSP00000513140.1:n.1408G>T
ENST00000697164.1:c.1488G>T	ENSP00000513153.1:p.Lys496Asn
ENST00000697165.1:c.1275G>T	ENSP00000513154.1:p.Lys425Asn
ENST00000347310.10:c.1578G>T MANE Select	ENSP00000321345.5:p.Lys526Asn
ENST00000637002.1:c.969G>T	ENSP00000490340.1:p.Lys323Asn
ENST00000347310.9:c.1578G>T	ENSP00000321345.5:p.Lys526Asn
ENST00000395227.2:c.372G>T	ENSP00000378652.2:p.Lys124Asn
ENST00000425614.3:c.813G>T	ENSP00000387640.2:p.Lys271Asn
ENST00000473881.2:c.*404G>T	ENSP00000486667.1:n.*404G>T
NM_144701.2:c.1578G>T	NP_653302.2:p.Lys526Asn
XM_005270516.2:c.816G>T	XP_005270573.1:p.Lys272Asn
XM_011540789.1:c.1668G>T	XP_011539091.1:p.Lys556Asn
XM_011540790.1:c.1578G>T	XP_011539092.1:p.Lys526Asn
XM_011540791.1:c.1578G>T	XP_011539093.1:p.Lys526Asn
XM_011540790.3:c.1578G>T	XP_011539092.1:p.Lys526Asn
XM_011540791.3:c.1578G>T	XP_011539093.1:p.Lys526Asn
XR_001736993.1:n.1658G>T
NM_144701.3:c.1578G>T MANE Select	NP_653302.2:p.Lys526Asn