Canonical Allele Identifier: CA53700995

Gene: IL1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112835941G>A , CM000664.2:g.112835941G>A	GRCh38
NC_000002.11:g.113593518G>A , CM000664.1:g.113593518G>A	GRCh37
NC_000002.10:g.113309989G>A	NCBI36
NG_008851.1:g.5839C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.47+242C>T MANE Select	ENSP00000263341.2:n.47+242C>T
ENST00000263341.6:c.47+242C>T	ENSP00000263341.2:n.47+242C>T
ENST00000416750.1:c.47+242C>T	ENSP00000400854.1:n.47+242C>T
ENST00000418817.5:c.47+242C>T	ENSP00000407219.1:n.47+242C>T
ENST00000432018.5:c.47+242C>T	ENSP00000409680.1:n.47+242C>T
ENST00000477398.1:n.134+242C>T
ENST00000491056.5:n.597+242C>T
ENST00000496280.5:n.134+242C>T
NM_000576.2:c.47+242C>T	NP_000567.1:n.47+242C>T
XM_006712496.1:c.-445+242C>T	XP_006712559.1:n.-445+242C>T
XM_017003988.2:c.-46-324C>T	XP_016859477.1:n.-46-324C>T
NM_000576.3:c.47+242C>T MANE Select	NP_000567.1:n.47+242C>T