Canonical Allele Identifier: CA535595900

Gene: IL1B

Linked Data

• dbSNP Id: rs1452359049
• gnomAD v2: 2-113588322-CCTT-C
• gnomAD v3: 2-112830745-CCTT-C
• gnomAD v4: 2-112830745-CCTT-C
• MyVariant Identifiers: chr2:g.113588323_113588325del (hg19) ; chr2:g.112830746_112830748del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830752_112830754del , CM000664.2:g.112830752_112830754del	GRCh38
NC_000002.11:g.113588329_113588331del , CM000664.1:g.113588329_113588331del	GRCh37
NC_000002.10:g.113304800_113304802del	NCBI36
NG_008851.1:g.11032_11034del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.598-175_598-173del MANE Select	ENSP00000263341.2:n.598-175_598-173del
ENST00000263341.6:c.598-175_598-173del	ENSP00000263341.2:n.598-175_598-173del
ENST00000491056.5:n.1405-175_1405-173del
NM_000576.2:c.598-175_598-173del	NP_000567.1:n.598-175_598-173del
XM_006712496.1:c.364-175_364-173del	XP_006712559.1:n.364-175_364-173del
XM_017003988.2:c.505-175_505-173del	XP_016859477.1:n.505-175_505-173del
NM_000576.3:c.598-175_598-173del MANE Select	NP_000567.1:n.598-175_598-173del