Canonical Allele Identifier: CA738095389

Gene: IL23R

Linked Data

• dbSNP Id: rs1351112441
• gnomAD v3: 1-67259576-T-A
• gnomAD v4: 1-67259576-T-A
• MyVariant Identifiers: chr1:g.67725259T>A (hg19) ; chr1:g.67259576T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259576T>A , CM000663.2:g.67259576T>A	GRCh38
NC_000001.10:g.67725259T>A , CM000663.1:g.67725259T>A	GRCh37
NC_000001.9:g.67497847T>A	NCBI36
NG_011498.1:g.98091T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*448T>A MANE Select	ENSP00000321345.5:n.*448T>A
ENST00000347310.9:c.*448T>A	ENSP00000321345.5:n.*448T>A
ENST00000395227.2:c.*448T>A	ENSP00000378652.2:n.*448T>A
ENST00000473881.2:c.*1164T>A	ENSP00000486667.1:n.*1164T>A
NM_144701.2:c.*448T>A	NP_653302.2:n.*448T>A
XM_005270516.2:c.*448T>A	XP_005270573.1:n.*448T>A
XM_011540789.1:c.*448T>A	XP_011539091.1:n.*448T>A
XM_011540790.1:c.*448T>A	XP_011539092.1:n.*448T>A
XM_011540791.1:c.*448T>A	XP_011539093.1:n.*448T>A
XM_011540790.3:c.*448T>A	XP_011539092.1:n.*448T>A
XM_011540791.3:c.*448T>A	XP_011539093.1:n.*448T>A
NM_144701.3:c.*448T>A MANE Select	NP_653302.2:n.*448T>A