Canonical Allele Identifier: CA1279938998
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1682008018
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832622C>A , CM000664.2:g.112832622C>A GRCh38
NC_000002.11:g.113590199C>A , CM000664.1:g.113590199C>A GRCh37
NC_000002.10:g.113306670C>A NCBI36
NG_008851.1:g.9158G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+40G>T MANE Select ENSP00000263341.2:n.466+40G>T
ENST00000263341.6:c.466+40G>T ENSP00000263341.2:n.466+40G>T
ENST00000487639.1:n.367+40G>T
ENST00000491056.5:n.1273+40G>T
NM_000576.2:c.466+40G>T NP_000567.1:n.466+40G>T
XM_006712496.1:c.232+40G>T XP_006712559.1:n.232+40G>T
XM_017003988.2:c.373+40G>T XP_016859477.1:n.373+40G>T
NM_000576.3:c.466+40G>T MANE Select NP_000567.1:n.466+40G>T
Search 100 bp 5'
Search 100 bp 3'