Canonical Allele Identifier: CA534999811
Gene: IL18R1 HGNC NCBI

Linked Data

dbSNP Id: rs1238304210
gnomAD v2: 2-102971837-T-C
gnomAD v3: 2-102355377-T-C
gnomAD v4: 2-102355377-T-C
MyVariant Identifiers: chr2:g.102971837T>C (hg19) chr2:g.102355377T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102355377T>C , CM000664.2:g.102355377T>C GRCh38
NC_000002.11:g.102971837T>C , CM000664.1:g.102971837T>C GRCh37
NC_000002.10:g.102338269T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410040.5:c.-28-7256T>C ENSP00000386663.1:n.-28-7256T>C
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