Canonical Allele Identifier: CA2751743880

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112831140_112831141insTACAAGACCGATGCAACGATGGCCAATCCGGAAACGGGCTATTTCACCGCTAAACCCACCACGGTGGAAAGCGTGCGCTTCGGTGCAGACGGTGCGCAGC , CM000664.2:g.112831140_112831141insTACAAGACCGATGCAACGATGGCCAATCCGGAAACGGGCTATTTCACCGCTAAACCCACCACGGTGGAAAGCGTGCGCTTCGGTGCAGACGGTGCGCAGC	GRCh38
NC_000002.11:g.113588717_113588718insTACAAGACCGATGCAACGATGGCCAATCCGGAAACGGGCTATTTCACCGCTAAACCCACCACGGTGGAAAGCGTGCGCTTCGGTGCAGACGGTGCGCAGC , CM000664.1:g.113588717_113588718insTACAAGACCGATGCAACGATGGCCAATCCGGAAACGGGCTATTTCACCGCTAAACCCACCACGGTGGAAAGCGTGCGCTTCGGTGCAGACGGTGCGCAGC	GRCh37
NC_000002.10:g.113305188_113305189insTACAAGACCGATGCAACGATGGCCAATCCGGAAACGGGCTATTTCACCGCTAAACCCACCACGGTGGAAAGCGTGCGCTTCGGTGCAGACGGTGCGCAGC	NCBI36
NG_008851.1:g.10639_10640insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.597+151_597+152insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA MANE Select	ENSP00000263341.2:n.597+151_597+152insGCT...
ENST00000263341.6:c.597+151_597+152insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA	ENSP00000263341.2:n.597+151_597+152insGCT...
ENST00000487639.1:n.649_650insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA
ENST00000491056.5:n.1404+151_1404+152insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA
NM_000576.2:c.597+151_597+152insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA	NP_000567.1:n.597+151_597+152insGCTGCGCAC...
XM_006712496.1:c.363+151_363+152insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA	XP_006712559.1:n.363+151_363+152insGCTGCG...
XM_017003988.2:c.504+151_504+152insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA	XP_016859477.1:n.504+151_504+152insGCTGCG...
NM_000576.3:c.597+151_597+152insGCTGCGCACCGTCTGCACCGAAGCGCACGCTTTCCACCGTGGTGGGTTTAGCGGTGAAATAGCCCGTTTCCGGATTGGCCATCGTTGCATCGGTCTTGTA MANE Select	NP_000567.1:n.597+151_597+152insGCTGCGCAC...