Canonical Allele Identifier: CA1279939008
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1682008344
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832641_112832642dup , CM000664.2:g.112832641_112832642dup GRCh38
NC_000002.11:g.113590218_113590219dup , CM000664.1:g.113590218_113590219dup GRCh37
NC_000002.10:g.113306689_113306690dup NCBI36
NG_008851.1:g.9139_9140dup

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+21_466+22dup MANE Select ENSP00000263341.2:n.466+21_466+22dup
ENST00000263341.6:c.466+21_466+22dup ENSP00000263341.2:n.466+21_466+22dup
ENST00000487639.1:n.367+21_367+22dup
ENST00000491056.5:n.1273+21_1273+22dup
NM_000576.2:c.466+21_466+22dup NP_000567.1:n.466+21_466+22dup
XM_006712496.1:c.232+21_232+22dup XP_006712559.1:n.232+21_232+22dup
XM_017003988.2:c.373+21_373+22dup XP_016859477.1:n.373+21_373+22dup
NM_000576.3:c.466+21_466+22dup MANE Select NP_000567.1:n.466+21_466+22dup
Search 100 bp 5'
Search 100 bp 3'