Canonical Allele Identifier: CA1279939954

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112834786C= , CM000664.2:g.112834786C=	GRCh38
NC_000002.11:g.113592363C= , CM000664.1:g.113592363C=	GRCh37
NC_000002.10:g.113308834C=	NCBI36
NG_008851.1:g.6994G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.99+780G= MANE Select	ENSP00000263341.2:n.99+780G=
ENST00000263341.6:c.99+780G=	ENSP00000263341.2:n.99+780G=
ENST00000416750.1:c.99+780G=	ENSP00000400854.1:n.99+780G=
ENST00000418817.5:c.99+780G=	ENSP00000407219.1:n.99+780G=
ENST00000432018.5:c.99+780G=	ENSP00000409680.1:n.99+780G=
ENST00000491056.5:n.649+780G=
ENST00000496280.5:n.186+780G=
NM_000576.2:c.99+780G=	NP_000567.1:n.99+780G=
XM_006712496.1:c.-393+780G=	XP_006712559.1:n.-393+780G=
XM_017003988.2:c.6+780G=	XP_016859477.1:n.6+780G=
NM_000576.3:c.99+780G= MANE Select	NP_000567.1:n.99+780G=