Canonical Allele Identifier: CA1279938191

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830551G= , CM000664.2:g.112830551G=	GRCh38
NC_000002.11:g.113588128G= , CM000664.1:g.113588128G=	GRCh37
NC_000002.10:g.113304599G=	NCBI36
NG_008851.1:g.11229C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.620C= MANE Select	ENSP00000263341.2:p.Pro207=
ENST00000263341.6:c.620C=	ENSP00000263341.2:p.Pro207=
ENST00000491056.5:n.1427C=
NM_000576.2:c.620C=	NP_000567.1:p.Pro207=
XM_006712496.1:c.386C=	XP_006712559.1:p.Pro129=
XM_017003988.2:c.527C=	XP_016859477.1:p.Pro176=
NM_000576.3:c.620C= MANE Select	NP_000567.1:p.Pro207=