Canonical Allele Identifier: CA15200971
Gene: IL1RL1 HGNC NCBI
IL18R1 HGNC NCBI
COSMIC:
COSN6671286 (not active)
MyVariant.info:
GRCh38 chr2:g.102337157G>T
GRCh37 chr2:g.102953617G>T
gnomAD v2:
2:102953617 G / T
gnomAD v3:
2:102337157 G / T
gnomAD v4:
chr2-102337157-G-T
Joint Max Group AF 0.25933164 (AFR)
Genomes Max Group AF 0.25933164 (AFR)
Exomes Max Group AF 0.10519509 (EAS)
dbSNP:
3771180
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102337157G>T , CM000664.2:g.102337157G>T GRCh38
NC_000002.11:g.102953617G>T , CM000664.1:g.102953617G>T GRCh37
NC_000002.10:g.102320049G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000233954.6:c.-149-959G>T (IL1RL1) MANE Select ENSP00000233954.1:n.-149-959G>T
ENST00000233954.5:c.-149-959G>T (IL1RL1) ENSP00000233954.1:n.-149-959G>T
ENST00000311734.6:c.-330G>T (IL1RL1) ENSP00000310371.2:n.-330G>T
ENST00000404917.6:c.-146-1824G>T (IL1RL1) ENSP00000384822.2:n.-146-1824G>T
ENST00000410040.5:c.-28-25476G>T (IL18R1) ENSP00000386663.1:n.-28-25476G>T
ENST00000447231.5:c.-149-959G>T (IL1RL1) ENSP00000409437.1:n.-149-959G>T
ENST00000473175.1:n.96-959G>T (IL1RL1)
NM_001282408.1:c.-146-1824G>T (IL1RL1) NP_001269337.1:n.-146-1824G>T
NM_016232.4:c.-149-959G>T (IL1RL1) NP_057316.3:n.-149-959G>T
XM_011512151.1:c.-149-959G>T (IL1RL1) XP_011510453.1:n.-149-959G>T
NM_016232.5:c.-149-959G>T (IL1RL1) MANE Select NP_057316.3:n.-149-959G>T
NM_001282408.2:c.-146-1824G>T (IL1RL1) NP_001269337.1:n.-146-1824G>T
Search 100 bp 5'
Search 100 bp 3'