Canonical Allele Identifier: CA1279938190
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830550_112830553delinsTGGG , CM000664.2:g.112830550_112830553delinsTGGG GRCh38
NC_000002.11:g.113588127_113588130delinsTGGG , CM000664.1:g.113588127_113588130delinsTGGG GRCh37
NC_000002.10:g.113304598_113304601delinsTGGG NCBI36
NG_008851.1:g.11227_11230delinsCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.618_621delinsCCCA MANE Select ENSP00000263341.2:p.Tyr206=
ENST00000263341.6:c.618_621delinsCCCA ENSP00000263341.2:p.Tyr206=
ENST00000491056.5:n.1425_1428delinsCCCA
NM_000576.2:c.618_621delinsCCCA NP_000567.1:p.Tyr206=
XM_006712496.1:c.384_387delinsCCCA XP_006712559.1:p.Tyr128=
XM_017003988.2:c.525_528delinsCCCA XP_016859477.1:p.Tyr175=
NM_000576.3:c.618_621delinsCCCA MANE Select NP_000567.1:p.Tyr206=
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