Canonical Allele Identifier: CA348288444

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113590392A>G (hg19) ; chr2:g.112832815A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832815A>G , CM000664.2:g.112832815A>G	GRCh38
NC_000002.11:g.113590392A>G , CM000664.1:g.113590392A>G	GRCh37
NC_000002.10:g.113306863A>G	NCBI36
NG_008851.1:g.8965T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.313T>C MANE Select	ENSP00000263341.2:p.Phe105Leu
ENST00000263341.6:c.313T>C	ENSP00000263341.2:p.Phe105Leu
ENST00000416750.1:c.313T>C	ENSP00000400854.1:p.Phe105Leu
ENST00000418817.5:c.313T>C	ENSP00000407219.1:p.Phe105Leu
ENST00000432018.5:c.313T>C	ENSP00000409680.1:p.Phe105Leu
ENST00000487639.1:n.214T>C
ENST00000491056.5:n.1120T>C
NM_000576.2:c.313T>C	NP_000567.1:p.Phe105Leu
XM_006712496.1:c.79T>C	XP_006712559.1:p.Phe27Leu
XM_017003988.2:c.220T>C	XP_016859477.1:p.Phe74Leu
NM_000576.3:c.313T>C MANE Select	NP_000567.1:p.Phe105Leu