Canonical Allele Identifier: CA53696749

Gene: IL1B

Linked Data

• dbSNP Id: rs1009507329
• MyVariant Identifiers: chr2:g.113588721_113588722del (hg19) ; chr2:g.112831144_112831145del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112831145_112831146del , CM000664.2:g.112831145_112831146del	GRCh38
NC_000002.11:g.113588722_113588723del , CM000664.1:g.113588722_113588723del	GRCh37
NC_000002.10:g.113305193_113305194del	NCBI36
NG_008851.1:g.10635_10636del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.597+147_597+148del MANE Select	ENSP00000263341.2:n.597+147_597+148del
ENST00000263341.6:c.597+147_597+148del	ENSP00000263341.2:n.597+147_597+148del
ENST00000487639.1:n.645_646del
ENST00000491056.5:n.1404+147_1404+148del
NM_000576.2:c.597+147_597+148del	NP_000567.1:n.597+147_597+148del
XM_006712496.1:c.363+147_363+148del	XP_006712559.1:n.363+147_363+148del
XM_017003988.2:c.504+147_504+148del	XP_016859477.1:n.504+147_504+148del
NM_000576.3:c.597+147_597+148del MANE Select	NP_000567.1:n.597+147_597+148del