Canonical Allele Identifier: CA1279939119

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832890C= , CM000664.2:g.112832890C=	GRCh38
NC_000002.11:g.113590467C= , CM000664.1:g.113590467C=	GRCh37
NC_000002.10:g.113306938C=	NCBI36
NG_008851.1:g.8890G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000576.3:c.302-64G= MANE Select	NP_000567.1:n.302-64G=
ENST00000263341.7:c.302-64G= MANE Select	ENSP00000263341.2:n.302-64G=
NM_000576.2:c.302-64G=	NP_000567.1:n.302-64G=
ENST00000263341.6:c.302-64G=	ENSP00000263341.2:n.302-64G=
ENST00000416750.1:c.302-64G=	ENSP00000400854.1:n.302-64G=
ENST00000418817.5:c.302-64G=	ENSP00000407219.1:n.302-64G=
ENST00000432018.5:c.302-64G=	ENSP00000409680.1:n.302-64G=
ENST00000487639.1:n.203-64G=
ENST00000491056.5:n.1109-64G=
XM_006712496.1:c.68-64G=	XP_006712559.1:n.68-64G=
XM_017003988.2:c.209-64G=	XP_016859477.1:n.209-64G=