Canonical Allele Identifier: CA738095374

Gene: IL23R

Linked Data

• dbSNP Id: rs1190592787
• gnomAD v3: 1-67259541-A-T
• gnomAD v4: 1-67259541-A-T
• MyVariant Identifiers: chr1:g.67725224A>T (hg19) ; chr1:g.67259541A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259541A>T , CM000663.2:g.67259541A>T	GRCh38
NC_000001.10:g.67725224A>T , CM000663.1:g.67725224A>T	GRCh37
NC_000001.9:g.67497812A>T	NCBI36
NG_011498.1:g.98056A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*413A>T MANE Select	ENSP00000321345.5:n.*413A>T
ENST00000347310.9:c.*413A>T	ENSP00000321345.5:n.*413A>T
ENST00000395227.2:c.*413A>T	ENSP00000378652.2:n.*413A>T
ENST00000473881.2:c.*1129A>T	ENSP00000486667.1:n.*1129A>T
NM_144701.2:c.*413A>T	NP_653302.2:n.*413A>T
XM_005270516.2:c.*413A>T	XP_005270573.1:n.*413A>T
XM_011540789.1:c.*413A>T	XP_011539091.1:n.*413A>T
XM_011540790.1:c.*413A>T	XP_011539092.1:n.*413A>T
XM_011540791.1:c.*413A>T	XP_011539093.1:n.*413A>T
XM_011540790.3:c.*413A>T	XP_011539092.1:n.*413A>T
XM_011540791.3:c.*413A>T	XP_011539093.1:n.*413A>T
NM_144701.3:c.*413A>T MANE Select	NP_653302.2:n.*413A>T