Canonical Allele Identifier: CA348288441

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113590391A>C (hg19) ; chr2:g.112832814A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832814A>C , CM000664.2:g.112832814A>C	GRCh38
NC_000002.11:g.113590391A>C , CM000664.1:g.113590391A>C	GRCh37
NC_000002.10:g.113306862A>C	NCBI36
NG_008851.1:g.8966T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.314T>G MANE Select	ENSP00000263341.2:p.Phe105Cys
ENST00000263341.6:c.314T>G	ENSP00000263341.2:p.Phe105Cys
ENST00000416750.1:c.314T>G	ENSP00000400854.1:p.Phe105Cys
ENST00000418817.5:c.314T>G	ENSP00000407219.1:p.Phe105Cys
ENST00000432018.5:c.314T>G	ENSP00000409680.1:p.Phe105Cys
ENST00000487639.1:n.215T>G
ENST00000491056.5:n.1121T>G
NM_000576.2:c.314T>G	NP_000567.1:p.Phe105Cys
XM_006712496.1:c.80T>G	XP_006712559.1:p.Phe27Cys
XM_017003988.2:c.221T>G	XP_016859477.1:p.Phe74Cys
NM_000576.3:c.314T>G MANE Select	NP_000567.1:p.Phe105Cys