Canonical Allele Identifier: CA52916335

Gene: IL1RL1 IL18R1

Linked Data

• dbSNP Id: rs923393375
• MyVariant Identifiers: chr2:g.102945347C>T (hg19) ; chr2:g.102328887C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102328887C>T , CM000664.2:g.102328887C>T	GRCh38
NC_000002.11:g.102945347C>T , CM000664.1:g.102945347C>T	GRCh37
NC_000002.10:g.102311779C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233954.6:c.-149-9229C>T (IL1RL1) MANE Select	ENSP00000233954.1:n.-149-9229C>T
ENST00000233954.5:c.-149-9229C>T (IL1RL1)	ENSP00000233954.1:n.-149-9229C>T
ENST00000404917.6:c.-146-10094C>T (IL1RL1)	ENSP00000384822.2:n.-146-10094C>T
ENST00000410040.5:c.-29+17264C>T (IL18R1)	ENSP00000386663.1:n.-29+17264C>T
ENST00000447231.5:c.-149-9229C>T (IL1RL1)	ENSP00000409437.1:n.-149-9229C>T
ENST00000473175.1:n.96-9229C>T (IL1RL1)
NM_001282408.1:c.-146-10094C>T (IL1RL1)	NP_001269337.1:n.-146-10094C>T
NM_016232.4:c.-149-9229C>T (IL1RL1)	NP_057316.3:n.-149-9229C>T
XM_011512151.1:c.-149-9229C>T (IL1RL1)	XP_011510453.1:n.-149-9229C>T
NM_016232.5:c.-149-9229C>T (IL1RL1) MANE Select	NP_057316.3:n.-149-9229C>T
NM_001282408.2:c.-146-10094C>T (IL1RL1)	NP_001269337.1:n.-146-10094C>T