Canonical Allele Identifier: CA1279939007
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832639G= , CM000664.2:g.112832639G= GRCh38
NC_000002.11:g.113590216G= , CM000664.1:g.113590216G= GRCh37
NC_000002.10:g.113306687G= NCBI36
NG_008851.1:g.9141C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+23C= MANE Select ENSP00000263341.2:n.466+23C=
ENST00000263341.6:c.466+23C= ENSP00000263341.2:n.466+23C=
ENST00000487639.1:n.367+23C=
ENST00000491056.5:n.1273+23C=
NM_000576.2:c.466+23C= NP_000567.1:n.466+23C=
XM_006712496.1:c.232+23C= XP_006712559.1:n.232+23C=
XM_017003988.2:c.373+23C= XP_016859477.1:n.373+23C=
NM_000576.3:c.466+23C= MANE Select NP_000567.1:n.466+23C=
Search 100 bp 5'
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