Canonical Allele Identifier: CA1035137295
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v3: 2-112830537-CCATCTT-C
gnomAD v4: 2-112830537-CCATCTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830539_112830544del , CM000664.2:g.112830539_112830544del GRCh38
NC_000002.11:g.113588116_113588121del , CM000664.1:g.113588116_113588121del GRCh37
NC_000002.10:g.113304587_113304592del NCBI36
NG_008851.1:g.11237_11242del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.628_633del MANE Select ENSP00000263341.2:p.Lys210_Met211del
ENST00000263341.6:c.628_633del ENSP00000263341.2:p.Lys210_Met211del
ENST00000491056.5:n.1435_1440del
NM_000576.2:c.628_633del NP_000567.1:p.Lys210_Met211del
XM_006712496.1:c.394_399del XP_006712559.1:p.Lys132_Met133del
XM_017003988.2:c.535_540del XP_016859477.1:p.Lys179_Met180del
NM_000576.3:c.628_633del MANE Select NP_000567.1:p.Lys210_Met211del
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