Canonical Allele Identifier: CA1279938388
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831018T= , CM000664.2:g.112831018T= GRCh38
NC_000002.11:g.113588595T= , CM000664.1:g.113588595T= GRCh37
NC_000002.10:g.113305066T= NCBI36
NG_008851.1:g.10762A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.597+274A= MANE Select ENSP00000263341.2:n.597+274A=
ENST00000263341.6:c.597+274A= ENSP00000263341.2:n.597+274A=
ENST00000491056.5:n.1404+274A=
NM_000576.2:c.597+274A= NP_000567.1:n.597+274A=
XM_006712496.1:c.363+274A= XP_006712559.1:n.363+274A=
XM_017003988.2:c.504+274A= XP_016859477.1:n.504+274A=
NM_000576.3:c.597+274A= MANE Select NP_000567.1:n.597+274A=
Search 100 bp 5'
Search 100 bp 3'