Canonical Allele Identifier: CA15176767

Gene: IL1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112834078T>G , CM000664.2:g.112834078T>G	GRCh38
NC_000002.11:g.113591655T>G , CM000664.1:g.113591655T>G	GRCh37
NC_000002.10:g.113308126T>G	NCBI36
NG_008851.1:g.7702A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.100-503A>C MANE Select	ENSP00000263341.2:n.100-503A>C
ENST00000263341.6:c.100-503A>C	ENSP00000263341.2:n.100-503A>C
ENST00000416750.1:c.100-503A>C	ENSP00000400854.1:n.100-503A>C
ENST00000418817.5:c.100-503A>C	ENSP00000407219.1:n.100-503A>C
ENST00000432018.5:c.100-503A>C	ENSP00000409680.1:n.100-503A>C
ENST00000491056.5:n.650-503A>C
ENST00000496280.5:n.187-503A>C
NM_000576.2:c.100-503A>C	NP_000567.1:n.100-503A>C
XM_006712496.1:c.-392-503A>C	XP_006712559.1:n.-392-503A>C
XM_017003988.2:c.7-503A>C	XP_016859477.1:n.7-503A>C
NM_000576.3:c.100-503A>C MANE Select	NP_000567.1:n.100-503A>C