Canonical Allele Identifier: CA348288449

Gene: IL1B

Linked Data

• gnomAD v4: 2-112832817-A-G
• MyVariant Identifiers: chr2:g.113590394A>G (hg19) ; chr2:g.112832817A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832817A>G , CM000664.2:g.112832817A>G	GRCh38
NC_000002.11:g.113590394A>G , CM000664.1:g.113590394A>G	GRCh37
NC_000002.10:g.113306865A>G	NCBI36
NG_008851.1:g.8963T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.311T>C MANE Select	ENSP00000263341.2:p.Phe104Ser
ENST00000263341.6:c.311T>C	ENSP00000263341.2:p.Phe104Ser
ENST00000416750.1:c.311T>C	ENSP00000400854.1:p.Phe104Ser
ENST00000418817.5:c.311T>C	ENSP00000407219.1:p.Phe104Ser
ENST00000432018.5:c.311T>C	ENSP00000409680.1:p.Phe104Ser
ENST00000487639.1:n.212T>C
ENST00000491056.5:n.1118T>C
NM_000576.2:c.311T>C	NP_000567.1:p.Phe104Ser
XM_006712496.1:c.77T>C	XP_006712559.1:p.Phe26Ser
XM_017003988.2:c.218T>C	XP_016859477.1:p.Phe73Ser
NM_000576.3:c.311T>C MANE Select	NP_000567.1:p.Phe104Ser