Canonical Allele Identifier: CA2577073793
Gene: IL1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830651del , CM000664.2:g.112830651del GRCh38
NC_000002.11:g.113588228del , CM000664.1:g.113588228del GRCh37
NC_000002.10:g.113304699del NCBI36
NG_008851.1:g.11130del

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.598-77del MANE Select ENSP00000263341.2:n.598-77del
ENST00000263341.6:c.598-77del ENSP00000263341.2:n.598-77del
ENST00000491056.5:n.1405-77del
NM_000576.2:c.598-77del NP_000567.1:n.598-77del
XM_006712496.1:c.364-77del XP_006712559.1:n.364-77del
XM_017003988.2:c.505-77del XP_016859477.1:n.505-77del
NM_000576.3:c.598-77del MANE Select NP_000567.1:n.598-77del