Canonical Allele Identifier: CA11076650
Gene: IL18R1 HGNC NCBI
COSMIC:
COSN6671313 (not active)
MyVariant.info:
GRCh38 chr2:g.102355405G>T
GRCh37 chr2:g.102971865G>T
gnomAD v2:
2:102971865 G / T
gnomAD v3:
2:102355405 G / T
gnomAD v4:
chr2-102355405-G-T
Joint Max Group AF 0.86242298 (AFR)
Genomes Max Group AF 0.86242298 (AFR)
dbSNP:
13015714
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102355405G>T , CM000664.2:g.102355405G>T GRCh38
NC_000002.11:g.102971865G>T , CM000664.1:g.102971865G>T GRCh37
NC_000002.10:g.102338297G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410040.5:c.-28-7228G>T ENSP00000386663.1:n.-28-7228G>T
Search 100 bp 5'
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