Canonical Allele Identifier: CA2751743879

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112831137_112831138insGAAGGGCGTAGTTGCCTACGAC , CM000664.2:g.112831137_112831138insGAAGGGCGTAGTTGCCTACGAC	GRCh38
NC_000002.11:g.113588714_113588715insGAAGGGCGTAGTTGCCTACGAC , CM000664.1:g.113588714_113588715insGAAGGGCGTAGTTGCCTACGAC	GRCh37
NC_000002.10:g.113305185_113305186insGAAGGGCGTAGTTGCCTACGAC	NCBI36
NG_008851.1:g.10642_10643insGTCGTAGGCAACTACGCCCTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.597+154_597+155insGTCGTAGGCAACTACGCCCTTC MANE Select	ENSP00000263341.2:n.597+154_597+155insGTC...
ENST00000263341.6:c.597+154_597+155insGTCGTAGGCAACTACGCCCTTC	ENSP00000263341.2:n.597+154_597+155insGTC...
ENST00000487639.1:n.652_653insGTCGTAGGCAACTACGCCCTTC
ENST00000491056.5:n.1404+154_1404+155insGTCGTAGGCAACTACGCCCTTC
NM_000576.2:c.597+154_597+155insGTCGTAGGCAACTACGCCCTTC	NP_000567.1:n.597+154_597+155insGTCGTAGGC...
XM_006712496.1:c.363+154_363+155insGTCGTAGGCAACTACGCCCTTC	XP_006712559.1:n.363+154_363+155insGTCGTA...
XM_017003988.2:c.504+154_504+155insGTCGTAGGCAACTACGCCCTTC	XP_016859477.1:n.504+154_504+155insGTCGTA...
NM_000576.3:c.597+154_597+155insGTCGTAGGCAACTACGCCCTTC MANE Select	NP_000567.1:n.597+154_597+155insGTCGTAGGC...