Canonical Allele Identifier: CA2660746889
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112830724-CCG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830725_112830726del , CM000664.2:g.112830725_112830726del GRCh38
NC_000002.11:g.113588302_113588303del , CM000664.1:g.113588302_113588303del GRCh37
NC_000002.10:g.113304773_113304774del NCBI36
NG_008851.1:g.11054_11055del

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.598-153_598-152del MANE Select ENSP00000263341.2:n.598-153_598-152del
ENST00000263341.6:c.598-153_598-152del ENSP00000263341.2:n.598-153_598-152del
ENST00000491056.5:n.1405-153_1405-152del
NM_000576.2:c.598-153_598-152del NP_000567.1:n.598-153_598-152del
XM_006712496.1:c.364-153_364-152del XP_006712559.1:n.364-153_364-152del
XM_017003988.2:c.505-153_505-152del XP_016859477.1:n.505-153_505-152del
NM_000576.3:c.598-153_598-152del MANE Select NP_000567.1:n.598-153_598-152del
Search 100 bp 5'
Search 100 bp 3'