Canonical Allele Identifier: CA348288440

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113590390G>T (hg19) ; chr2:g.112832813G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832813G>T , CM000664.2:g.112832813G>T	GRCh38
NC_000002.11:g.113590390G>T , CM000664.1:g.113590390G>T	GRCh37
NC_000002.10:g.113306861G>T	NCBI36
NG_008851.1:g.8967C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.315C>A MANE Select	ENSP00000263341.2:p.Phe105Leu
ENST00000263341.6:c.315C>A	ENSP00000263341.2:p.Phe105Leu
ENST00000416750.1:c.315C>A	ENSP00000400854.1:p.Phe105Leu
ENST00000418817.5:c.315C>A	ENSP00000407219.1:p.Phe105Leu
ENST00000432018.5:c.315C>A	ENSP00000409680.1:p.Phe105Leu
ENST00000487639.1:n.216C>A
ENST00000491056.5:n.1122C>A
NM_000576.2:c.315C>A	NP_000567.1:p.Phe105Leu
XM_006712496.1:c.81C>A	XP_006712559.1:p.Phe27Leu
XM_017003988.2:c.222C>A	XP_016859477.1:p.Phe74Leu
NM_000576.3:c.315C>A MANE Select	NP_000567.1:p.Phe105Leu