Canonical Allele Identifier: CA2751743957
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832638G>A , CM000664.2:g.112832638G>A GRCh38
NC_000002.11:g.113590215G>A , CM000664.1:g.113590215G>A GRCh37
NC_000002.10:g.113306686G>A NCBI36
NG_008851.1:g.9142C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+24C>T MANE Select ENSP00000263341.2:n.466+24C>T
ENST00000263341.6:c.466+24C>T ENSP00000263341.2:n.466+24C>T
ENST00000487639.1:n.367+24C>T
ENST00000491056.5:n.1273+24C>T
NM_000576.2:c.466+24C>T NP_000567.1:n.466+24C>T
XM_006712496.1:c.232+24C>T XP_006712559.1:n.232+24C>T
XM_017003988.2:c.373+24C>T XP_016859477.1:n.373+24C>T
NM_000576.3:c.466+24C>T MANE Select NP_000567.1:n.466+24C>T
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