Canonical Allele Identifier: CA755285992
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1325425136
gnomAD v4: 2-112836817-A-C
MyVariant Identifiers: chr2:g.113594394A>C (hg19) chr2:g.112836817A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112836817A>C , CM000664.2:g.112836817A>C GRCh38
NC_000002.11:g.113594394A>C , CM000664.1:g.113594394A>C GRCh37
NC_000002.10:g.113310865A>C NCBI36
NG_008851.1:g.4963T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.6:c.-125T>G ENSP00000263341.2:n.-125T>G
XM_017003988.2:c.-156T>G XP_016859477.1:n.-156T>G
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