Canonical Allele Identifier: CA1279938255
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830705T= , CM000664.2:g.112830705T= GRCh38
NC_000002.11:g.113588282T= , CM000664.1:g.113588282T= GRCh37
NC_000002.10:g.113304753T= NCBI36
NG_008851.1:g.11075A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-132A= MANE Select ENSP00000263341.2:n.598-132A=
ENST00000263341.6:c.598-132A= ENSP00000263341.2:n.598-132A=
ENST00000491056.5:n.1405-132A=
NM_000576.2:c.598-132A= NP_000567.1:n.598-132A=
XM_006712496.1:c.364-132A= XP_006712559.1:n.364-132A=
XM_017003988.2:c.505-132A= XP_016859477.1:n.505-132A=
NM_000576.3:c.598-132A= MANE Select NP_000567.1:n.598-132A=
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