Canonical Allele Identifier: CA2751743842
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830592A>T , CM000664.2:g.112830592A>T GRCh38
NC_000002.11:g.113588169A>T , CM000664.1:g.113588169A>T GRCh37
NC_000002.10:g.113304640A>T NCBI36
NG_008851.1:g.11188T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-19T>A MANE Select ENSP00000263341.2:n.598-19T>A
ENST00000263341.6:c.598-19T>A ENSP00000263341.2:n.598-19T>A
ENST00000491056.5:n.1405-19T>A
NM_000576.2:c.598-19T>A NP_000567.1:n.598-19T>A
XM_006712496.1:c.364-19T>A XP_006712559.1:n.364-19T>A
XM_017003988.2:c.505-19T>A XP_016859477.1:n.505-19T>A
NM_000576.3:c.598-19T>A MANE Select NP_000567.1:n.598-19T>A
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