Canonical Allele Identifier: CA2700331344
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs2104934090

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830712del , CM000664.2:g.112830712del GRCh38
NC_000002.11:g.113588289del , CM000664.1:g.113588289del GRCh37
NC_000002.10:g.113304760del NCBI36
NG_008851.1:g.11070del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-137del MANE Select ENSP00000263341.2:n.598-137del
ENST00000263341.6:c.598-137del ENSP00000263341.2:n.598-137del
ENST00000491056.5:n.1405-137del
NM_000576.2:c.598-137del NP_000567.1:n.598-137del
XM_006712496.1:c.364-137del XP_006712559.1:n.364-137del
XM_017003988.2:c.505-137del XP_016859477.1:n.505-137del
NM_000576.3:c.598-137del MANE Select NP_000567.1:n.598-137del