Canonical Allele Identifier: CA1279939087
Gene: IL1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832821T= , CM000664.2:g.112832821T= GRCh38
NC_000002.11:g.113590398T= , CM000664.1:g.113590398T= GRCh37
NC_000002.10:g.113306869T= NCBI36
NG_008851.1:g.8959A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.307A= MANE Select ENSP00000263341.2:p.Ile103=
ENST00000263341.6:c.307A= ENSP00000263341.2:p.Ile103=
ENST00000416750.1:c.307A= ENSP00000400854.1:p.Ile103=
ENST00000418817.5:c.307A= ENSP00000407219.1:p.Ile103=
ENST00000432018.5:c.307A= ENSP00000409680.1:p.Ile103=
ENST00000487639.1:n.208A=
ENST00000491056.5:n.1114A=
NM_000576.2:c.307A= NP_000567.1:p.Ile103=
XM_006712496.1:c.73A= XP_006712559.1:p.Ile25=
XM_017003988.2:c.214A= XP_016859477.1:p.Ile72=
NM_000576.3:c.307A= MANE Select NP_000567.1:p.Ile103=