Canonical Allele Identifier: CA1279938273
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830758_112830759delinsTA , CM000664.2:g.112830758_112830759delinsTA GRCh38
NC_000002.11:g.113588335_113588336delinsTA , CM000664.1:g.113588335_113588336delinsTA GRCh37
NC_000002.10:g.113304806_113304807delinsTA NCBI36
NG_008851.1:g.11021_11022delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-186_598-185delinsTA MANE Select ENSP00000263341.2:n.598-186_598-185delinsTA
ENST00000263341.6:c.598-186_598-185delinsTA ENSP00000263341.2:n.598-186_598-185delinsTA
ENST00000491056.5:n.1405-186_1405-185delinsTA
NM_000576.2:c.598-186_598-185delinsTA NP_000567.1:n.598-186_598-185delinsTA
XM_006712496.1:c.364-186_364-185delinsTA XP_006712559.1:n.364-186_364-185delinsTA
XM_017003988.2:c.505-186_505-185delinsTA XP_016859477.1:n.505-186_505-185delinsTA
NM_000576.3:c.598-186_598-185delinsTA MANE Select NP_000567.1:n.598-186_598-185delinsTA
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