Canonical Allele Identifier: CA523280303

Gene: IL23R C1orf141

Linked Data

• dbSNP Id: rs1199414088
• gnomAD v2: 1-67633793-T-C
• gnomAD v4: 1-67168110-T-C
• MyVariant Identifiers: chr1:g.67633793T>C (hg19) ; chr1:g.67168110T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67168110T>C , CM000663.2:g.67168110T>C	GRCh38
NC_000001.10:g.67633793T>C , CM000663.1:g.67633793T>C	GRCh37
NC_000001.9:g.67406381T>C	NCBI36
NG_011498.1:g.6625T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697222.1:c.-11T>C (IL23R)	ENSP00000513189.1:n.-11T>C
ENST00000347310.10:c.-11T>C (IL23R) MANE Select	ENSP00000321345.5:n.-11T>C
ENST00000637002.1:c.-615T>C (IL23R)	ENSP00000490340.1:n.-615T>C
ENST00000347310.9:c.-11T>C (IL23R)	ENSP00000321345.5:n.-11T>C
ENST00000371007.6:c.-103-36883A>G (C1orf141)	ENSP00000360046.1:n.-103-36883A>G
ENST00000448166.6:c.-103-36883A>G (C1orf141)	ENSP00000415519.2:n.-103-36883A>G
NM_144701.2:c.-11T>C (IL23R)	NP_653302.2:n.-11T>C
XM_011540789.1:c.80T>C (IL23R)	XP_011539091.1:p.Leu27Pro
XM_011540790.1:c.-11T>C (IL23R)	XP_011539092.1:n.-11T>C
XM_011540791.1:c.-11T>C (IL23R)	XP_011539093.1:n.-11T>C
XM_011540790.3:c.-11T>C (IL23R)	XP_011539092.1:n.-11T>C
XM_011540791.3:c.-11T>C (IL23R)	XP_011539093.1:n.-11T>C
XR_001736993.1:n.173T>C (IL23R)
NM_144701.3:c.-11T>C (IL23R) MANE Select	NP_653302.2:n.-11T>C