Canonical Allele Identifier: CA52932058
Gene: IL18R1 HGNC NCBI

Linked Data

dbSNP Id: rs964169763
MyVariant Identifiers: chr2:g.102355476A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102355476A>T , CM000664.2:g.102355476A>T GRCh38
NC_000002.11:g.102971936A>T , CM000664.1:g.102971936A>T GRCh37
NC_000002.10:g.102338368A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410040.5:c.-28-7157A>T ENSP00000386663.1:n.-28-7157A>T
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