Canonical Allele Identifier: CA1279939462

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112833698A= , CM000664.2:g.112833698A=	GRCh38
NC_000002.11:g.113591275A= , CM000664.1:g.113591275A=	GRCh37
NC_000002.10:g.113307746A=	NCBI36
NG_008851.1:g.8082T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.100-123T= MANE Select	ENSP00000263341.2:n.100-123T=
ENST00000263341.6:c.100-123T=	ENSP00000263341.2:n.100-123T=
ENST00000416750.1:c.100-123T=	ENSP00000400854.1:n.100-123T=
ENST00000418817.5:c.100-123T=	ENSP00000407219.1:n.100-123T=
ENST00000432018.5:c.100-123T=	ENSP00000409680.1:n.100-123T=
ENST00000491056.5:n.650-123T=
ENST00000496280.5:n.187-123T=
NM_000576.2:c.100-123T=	NP_000567.1:n.100-123T=
XM_006712496.1:c.-392-123T=	XP_006712559.1:n.-392-123T=
XM_017003988.2:c.7-123T=	XP_016859477.1:n.7-123T=
NM_000576.3:c.100-123T= MANE Select	NP_000567.1:n.100-123T=