Canonical Allele Identifier: CA52931948
Gene: IL18R1 HGNC NCBI

Linked Data

dbSNP Id: rs753909617
MyVariant Identifiers: chr2:g.102971691G>A (hg19) chr2:g.102355231G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102355231G>A , CM000664.2:g.102355231G>A GRCh38
NC_000002.11:g.102971691G>A , CM000664.1:g.102971691G>A GRCh37
NC_000002.10:g.102338123G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000410040.5:c.-28-7402G>A ENSP00000386663.1:n.-28-7402G>A
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