Canonical Allele Identifier: CA1279938231

Gene: IL1B

Linked Data

• dbSNP Id: rs777137031

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830632A>C , CM000664.2:g.112830632A>C	GRCh38
NC_000002.11:g.113588209A>C , CM000664.1:g.113588209A>C	GRCh37
NC_000002.10:g.113304680A>C	NCBI36
NG_008851.1:g.11148T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.598-59T>G MANE Select	ENSP00000263341.2:n.598-59T>G
ENST00000263341.6:c.598-59T>G	ENSP00000263341.2:n.598-59T>G
ENST00000491056.5:n.1405-59T>G
NM_000576.2:c.598-59T>G	NP_000567.1:n.598-59T>G
XM_006712496.1:c.364-59T>G	XP_006712559.1:n.364-59T>G
XM_017003988.2:c.505-59T>G	XP_016859477.1:n.505-59T>G
NM_000576.3:c.598-59T>G MANE Select	NP_000567.1:n.598-59T>G