Canonical Allele Identifier: CA2660746838
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112830700-A-ATCAT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830700_112830701insTCAT , CM000664.2:g.112830700_112830701insTCAT GRCh38
NC_000002.11:g.113588277_113588278insTCAT , CM000664.1:g.113588277_113588278insTCAT GRCh37
NC_000002.10:g.113304748_113304749insTCAT NCBI36
NG_008851.1:g.11079_11080insATGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-128_598-127insATGA MANE Select ENSP00000263341.2:n.598-128_598-127insATGA
ENST00000263341.6:c.598-128_598-127insATGA ENSP00000263341.2:n.598-128_598-127insATGA
ENST00000491056.5:n.1405-128_1405-127insATGA
NM_000576.2:c.598-128_598-127insATGA NP_000567.1:n.598-128_598-127insATGA
XM_006712496.1:c.364-128_364-127insATGA XP_006712559.1:n.364-128_364-127insATGA
XM_017003988.2:c.505-128_505-127insATGA XP_016859477.1:n.505-128_505-127insATGA
NM_000576.3:c.598-128_598-127insATGA MANE Select NP_000567.1:n.598-128_598-127insATGA
Search 100 bp 5'
Search 100 bp 3'