Canonical Allele Identifier: CA2660746751

Gene: IL1B

Linked Data

• gnomAD v4: 2-112830615-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830618del , CM000664.2:g.112830618del	GRCh38
NC_000002.11:g.113588195del , CM000664.1:g.113588195del	GRCh37
NC_000002.10:g.113304666del	NCBI36
NG_008851.1:g.11164del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-43del MANE Select	ENSP00000263341.2:n.598-43del
ENST00000263341.6:c.598-43del	ENSP00000263341.2:n.598-43del
ENST00000491056.5:n.1405-43del
NM_000576.2:c.598-43del	NP_000567.1:n.598-43del
XM_006712496.1:c.364-43del	XP_006712559.1:n.364-43del
XM_017003988.2:c.505-43del	XP_016859477.1:n.505-43del
NM_000576.3:c.598-43del MANE Select	NP_000567.1:n.598-43del