Canonical Allele Identifier: CA738109531

Gene: IL23R C1orf141

Linked Data

• dbSNP Id: rs1413024953
• gnomAD v3: 1-67165617-G-T
• gnomAD v4: 1-67165617-G-T
• MyVariant Identifiers: chr1:g.67631300G>T (hg19) ; chr1:g.67165617G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67165617G>T , CM000663.2:g.67165617G>T	GRCh38
NC_000001.10:g.67631300G>T , CM000663.1:g.67631300G>T	GRCh37
NC_000001.9:g.67403888G>T	NCBI36
NG_011498.1:g.4132G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697222.1:c.-29-2475G>T (IL23R)	ENSP00000513189.1:n.-29-2475G>T
ENST00000637002.1:c.-633-2475G>T (IL23R)	ENSP00000490340.1:n.-633-2475G>T
ENST00000371007.6:c.-103-34390C>A (C1orf141)	ENSP00000360046.1:n.-103-34390C>A
ENST00000448166.6:c.-103-34390C>A (C1orf141)	ENSP00000415519.2:n.-103-34390C>A
XM_011540789.1:c.62-2475G>T (IL23R)	XP_011539091.1:n.62-2475G>T
XM_011540790.1:c.-29-2475G>T (IL23R)	XP_011539092.1:n.-29-2475G>T
XM_011540791.1:c.-29-2475G>T (IL23R)	XP_011539093.1:n.-29-2475G>T
XM_011540790.3:c.-29-2475G>T (IL23R)	XP_011539092.1:n.-29-2475G>T
XM_011540791.3:c.-29-2475G>T (IL23R)	XP_011539093.1:n.-29-2475G>T