Canonical Allele Identifier: CA1034377798
Gene: IL1RL1 HGNC NCBI
IL18R1 HGNC NCBI

Linked Data

dbSNP Id: rs1573153979

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102341166A>T , CM000664.2:g.102341166A>T GRCh38
NC_000002.11:g.102957626A>T , CM000664.1:g.102957626A>T GRCh37
NC_000002.10:g.102324058A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000233954.6:c.610+338A>T (IL1RL1) MANE Select ENSP00000233954.1:n.610+338A>T
ENST00000233954.5:c.610+338A>T (IL1RL1) ENSP00000233954.1:n.610+338A>T
ENST00000311734.6:c.610+338A>T (IL1RL1) ENSP00000310371.2:n.610+338A>T
ENST00000404917.6:c.259+338A>T (IL1RL1) ENSP00000384822.2:n.259+338A>T
ENST00000409584.5:c.610+338A>T (IL1RL1) ENSP00000386618.1:n.610+338A>T
ENST00000410040.5:c.-28-21467A>T (IL18R1) ENSP00000386663.1:n.-28-21467A>T
ENST00000427077.1:c.611-22A>T (IL1RL1) ENSP00000391120.1:n.611-22A>T
ENST00000482701.5:n.443+894A>T (IL1RL1)
NM_001282408.1:c.259+338A>T (IL1RL1) NP_001269337.1:n.259+338A>T
NM_003856.3:c.610+338A>T (IL1RL1) NP_003847.2:n.610+338A>T
NM_016232.4:c.610+338A>T (IL1RL1) NP_057316.3:n.610+338A>T
NR_104167.1:n.848-22A>T (IL1RL1)
XM_006712839.2:c.610+338A>T (IL1RL1) XP_006712902.1:n.610+338A>T
XM_011512151.1:c.610+338A>T (IL1RL1) XP_011510453.1:n.610+338A>T
XM_006712839.3:c.610+338A>T (IL1RL1) XP_006712902.1:n.610+338A>T
NM_003856.4:c.610+338A>T (IL1RL1) NP_003847.2:n.610+338A>T
NM_016232.5:c.610+338A>T (IL1RL1) MANE Select NP_057316.3:n.610+338A>T
NR_104167.2:n.841-22A>T (IL1RL1)
NM_001282408.2:c.259+338A>T (IL1RL1) NP_001269337.1:n.259+338A>T