Canonical Allele Identifier: CA1279938268
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830743_112830744delinsGC , CM000664.2:g.112830743_112830744delinsGC GRCh38
NC_000002.11:g.113588320_113588321delinsGC , CM000664.1:g.113588320_113588321delinsGC GRCh37
NC_000002.10:g.113304791_113304792delinsGC NCBI36
NG_008851.1:g.11036_11037delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-171_598-170delinsGC MANE Select ENSP00000263341.2:n.598-171_598-170delinsGC
ENST00000263341.6:c.598-171_598-170delinsGC ENSP00000263341.2:n.598-171_598-170delinsGC
ENST00000491056.5:n.1405-171_1405-170delinsGC
NM_000576.2:c.598-171_598-170delinsGC NP_000567.1:n.598-171_598-170delinsGC
XM_006712496.1:c.364-171_364-170delinsGC XP_006712559.1:n.364-171_364-170delinsGC
XM_017003988.2:c.505-171_505-170delinsGC XP_016859477.1:n.505-171_505-170delinsGC
NM_000576.3:c.598-171_598-170delinsGC MANE Select NP_000567.1:n.598-171_598-170delinsGC
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