Canonical Allele Identifier: CA1279938473

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112831215_112831216delinsGC , CM000664.2:g.112831215_112831216delinsGC	GRCh38
NC_000002.11:g.113588792_113588793delinsGC , CM000664.1:g.113588792_113588793delinsGC	GRCh37
NC_000002.10:g.113305263_113305264delinsGC	NCBI36
NG_008851.1:g.10564_10565delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.597+76_597+77delinsGC MANE Select	ENSP00000263341.2:n.597+76_597+77delinsGC
ENST00000263341.6:c.597+76_597+77delinsGC	ENSP00000263341.2:n.597+76_597+77delinsGC
ENST00000487639.1:n.574_575delinsGC
ENST00000491056.5:n.1404+76_1404+77delinsGC
NM_000576.2:c.597+76_597+77delinsGC	NP_000567.1:n.597+76_597+77delinsGC
XM_006712496.1:c.363+76_363+77delinsGC	XP_006712559.1:n.363+76_363+77delinsGC
XM_017003988.2:c.504+76_504+77delinsGC	XP_016859477.1:n.504+76_504+77delinsGC
NM_000576.3:c.597+76_597+77delinsGC MANE Select	NP_000567.1:n.597+76_597+77delinsGC