Canonical Allele Identifier: CA754303773

Gene: IL1RL1 IL18R1

Linked Data

• dbSNP Id: rs1401941625
• MyVariant Identifiers: chr2:g.102945612T>C (hg19) ; chr2:g.102329152T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102329152T>C , CM000664.2:g.102329152T>C	GRCh38
NC_000002.11:g.102945612T>C , CM000664.1:g.102945612T>C	GRCh37
NC_000002.10:g.102312044T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233954.6:c.-149-8964T>C (IL1RL1) MANE Select	ENSP00000233954.1:n.-149-8964T>C
ENST00000233954.5:c.-149-8964T>C (IL1RL1)	ENSP00000233954.1:n.-149-8964T>C
ENST00000404917.6:c.-146-9829T>C (IL1RL1)	ENSP00000384822.2:n.-146-9829T>C
ENST00000410040.5:c.-29+17529T>C (IL18R1)	ENSP00000386663.1:n.-29+17529T>C
ENST00000447231.5:c.-149-8964T>C (IL1RL1)	ENSP00000409437.1:n.-149-8964T>C
ENST00000473175.1:n.96-8964T>C (IL1RL1)
NM_001282408.1:c.-146-9829T>C (IL1RL1)	NP_001269337.1:n.-146-9829T>C
NM_016232.4:c.-149-8964T>C (IL1RL1)	NP_057316.3:n.-149-8964T>C
XM_011512151.1:c.-149-8964T>C (IL1RL1)	XP_011510453.1:n.-149-8964T>C
NM_016232.5:c.-149-8964T>C (IL1RL1) MANE Select	NP_057316.3:n.-149-8964T>C
NM_001282408.2:c.-146-9829T>C (IL1RL1)	NP_001269337.1:n.-146-9829T>C