Canonical Allele Identifier: CA534999812
Gene: IL18R1 HGNC NCBI

Linked Data

dbSNP Id: rs1294178512
gnomAD v2: 2-102971838-G-C
gnomAD v3: 2-102355378-G-C
gnomAD v4: 2-102355378-G-C
MyVariant Identifiers: chr2:g.102971838G>C (hg19) chr2:g.102355378G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102355378G>C , CM000664.2:g.102355378G>C GRCh38
NC_000002.11:g.102971838G>C , CM000664.1:g.102971838G>C GRCh37
NC_000002.10:g.102338270G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410040.5:c.-28-7255G>C ENSP00000386663.1:n.-28-7255G>C
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