Canonical Allele Identifier: CA2660747230
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112832618-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832618G>T , CM000664.2:g.112832618G>T GRCh38
NC_000002.11:g.113590195G>T , CM000664.1:g.113590195G>T GRCh37
NC_000002.10:g.113306666G>T NCBI36
NG_008851.1:g.9162C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+44C>A MANE Select ENSP00000263341.2:n.466+44C>A
ENST00000263341.6:c.466+44C>A ENSP00000263341.2:n.466+44C>A
ENST00000487639.1:n.367+44C>A
ENST00000491056.5:n.1273+44C>A
NM_000576.2:c.466+44C>A NP_000567.1:n.466+44C>A
XM_006712496.1:c.232+44C>A XP_006712559.1:n.232+44C>A
XM_017003988.2:c.373+44C>A XP_016859477.1:n.373+44C>A
NM_000576.3:c.466+44C>A MANE Select NP_000567.1:n.466+44C>A
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