Canonical Allele Identifier: CA1279939090
Gene: IL1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832825T= , CM000664.2:g.112832825T= GRCh38
NC_000002.11:g.113590402T= , CM000664.1:g.113590402T= GRCh37
NC_000002.10:g.113306873T= NCBI36
NG_008851.1:g.8955A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.303A= MANE Select ENSP00000263341.2:p.Glu101=
ENST00000263341.6:c.303A= ENSP00000263341.2:p.Glu101=
ENST00000416750.1:c.303A= ENSP00000400854.1:p.Glu101=
ENST00000418817.5:c.303A= ENSP00000407219.1:p.Glu101=
ENST00000432018.5:c.303A= ENSP00000409680.1:p.Glu101=
ENST00000487639.1:n.204A=
ENST00000491056.5:n.1110A=
NM_000576.2:c.303A= NP_000567.1:p.Glu101=
XM_006712496.1:c.69A= XP_006712559.1:p.Glu23=
XM_017003988.2:c.210A= XP_016859477.1:p.Glu70=
NM_000576.3:c.303A= MANE Select NP_000567.1:p.Glu101=