Canonical Allele Identifier: CA1279939017
Gene: IL1B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832657T= , CM000664.2:g.112832657T= GRCh38
NC_000002.11:g.113590234T= , CM000664.1:g.113590234T= GRCh37
NC_000002.10:g.113306705T= NCBI36
NG_008851.1:g.9123A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+5A= MANE Select ENSP00000263341.2:n.466+5A=
ENST00000263341.6:c.466+5A= ENSP00000263341.2:n.466+5A=
ENST00000487639.1:n.367+5A=
ENST00000491056.5:n.1273+5A=
NM_000576.2:c.466+5A= NP_000567.1:n.466+5A=
XM_006712496.1:c.232+5A= XP_006712559.1:n.232+5A=
XM_017003988.2:c.373+5A= XP_016859477.1:n.373+5A=
NM_000576.3:c.466+5A= MANE Select NP_000567.1:n.466+5A=
Search 100 bp 5'
Search 100 bp 3'