Canonical Allele Identifier: CA535596008
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v2: 2-113588120-TC-T
gnomAD v3: 2-112830543-TC-T
gnomAD v4: 2-112830543-TC-T
MyVariant Identifiers: chr2:g.113588121_113588124delinsTTC (hg19) chr2:g.112830544_112830547delinsTTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830544del , CM000664.2:g.112830544del GRCh38
NC_000002.11:g.113588121del , CM000664.1:g.113588121del GRCh37
NC_000002.10:g.113304592del NCBI36
NG_008851.1:g.11236del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.627del MANE Select ENSP00000263341.2:p.Lys210ArgfsTer11
ENST00000263341.6:c.627del ENSP00000263341.2:p.Lys210ArgfsTer11
ENST00000491056.5:n.1434del
NM_000576.2:c.627del NP_000567.1:p.Lys210ArgfsTer11
XM_006712496.1:c.393del XP_006712559.1:p.Lys132ArgfsTer11
XM_017003988.2:c.534del XP_016859477.1:p.Lys179ArgfsTer11
NM_000576.3:c.627del MANE Select NP_000567.1:p.Lys210ArgfsTer11
Search 100 bp 5'
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