Canonical Allele Identifier: CA738095358

Gene: IL23R

Linked Data

• dbSNP Id: rs1300405558
• gnomAD v4: 1-67259496-T-A
• MyVariant Identifiers: chr1:g.67725179T>A (hg19) ; chr1:g.67259496T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259496T>A , CM000663.2:g.67259496T>A	GRCh38
NC_000001.10:g.67725179T>A , CM000663.1:g.67725179T>A	GRCh37
NC_000001.9:g.67497767T>A	NCBI36
NG_011498.1:g.98011T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*368T>A MANE Select	ENSP00000321345.5:n.*368T>A
ENST00000347310.9:c.*368T>A	ENSP00000321345.5:n.*368T>A
ENST00000395227.2:c.*368T>A	ENSP00000378652.2:n.*368T>A
ENST00000473881.2:c.*1084T>A	ENSP00000486667.1:n.*1084T>A
NM_144701.2:c.*368T>A	NP_653302.2:n.*368T>A
XM_005270516.2:c.*368T>A	XP_005270573.1:n.*368T>A
XM_011540789.1:c.*368T>A	XP_011539091.1:n.*368T>A
XM_011540790.1:c.*368T>A	XP_011539092.1:n.*368T>A
XM_011540791.1:c.*368T>A	XP_011539093.1:n.*368T>A
XM_011540790.3:c.*368T>A	XP_011539092.1:n.*368T>A
XM_011540791.3:c.*368T>A	XP_011539093.1:n.*368T>A
NM_144701.3:c.*368T>A MANE Select	NP_653302.2:n.*368T>A