Canonical Allele Identifier: CA1279938195

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830559T= , CM000664.2:g.112830559T=	GRCh38
NC_000002.11:g.113588136T= , CM000664.1:g.113588136T=	GRCh37
NC_000002.10:g.113304607T=	NCBI36
NG_008851.1:g.11221A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.612A= MANE Select	ENSP00000263341.2:p.Lys204=
ENST00000263341.6:c.612A=	ENSP00000263341.2:p.Lys204=
ENST00000491056.5:n.1419A=
NM_000576.2:c.612A=	NP_000567.1:p.Lys204=
XM_006712496.1:c.378A=	XP_006712559.1:p.Lys126=
XM_017003988.2:c.519A=	XP_016859477.1:p.Lys173=
NM_000576.3:c.612A= MANE Select	NP_000567.1:p.Lys204=