Canonical Allele Identifier: CA1279938230
Gene: IL1B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830632A= , CM000664.2:g.112830632A= GRCh38
NC_000002.11:g.113588209A= , CM000664.1:g.113588209A= GRCh37
NC_000002.10:g.113304680A= NCBI36
NG_008851.1:g.11148T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-59T= MANE Select ENSP00000263341.2:n.598-59T=
ENST00000263341.6:c.598-59T= ENSP00000263341.2:n.598-59T=
ENST00000491056.5:n.1405-59T=
NM_000576.2:c.598-59T= NP_000567.1:n.598-59T=
XM_006712496.1:c.364-59T= XP_006712559.1:n.364-59T=
XM_017003988.2:c.505-59T= XP_016859477.1:n.505-59T=
NM_000576.3:c.598-59T= MANE Select NP_000567.1:n.598-59T=
Search 100 bp 5'
Search 100 bp 3'