Canonical Allele Identifier: CA15178075

Gene: IL1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830976A>G , CM000664.2:g.112830976A>G	GRCh38
NC_000002.11:g.113588553A>G , CM000664.1:g.113588553A>G	GRCh37
NC_000002.10:g.113305024A>G	NCBI36
NG_008851.1:g.10804T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.597+316T>C MANE Select	ENSP00000263341.2:n.597+316T>C
ENST00000263341.6:c.597+316T>C	ENSP00000263341.2:n.597+316T>C
ENST00000491056.5:n.1404+316T>C
NM_000576.2:c.597+316T>C	NP_000567.1:n.597+316T>C
XM_006712496.1:c.363+316T>C	XP_006712559.1:n.363+316T>C
XM_017003988.2:c.504+316T>C	XP_016859477.1:n.504+316T>C
NM_000576.3:c.597+316T>C MANE Select	NP_000567.1:n.597+316T>C