Canonical Allele Identifier: CA535596006
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1256379355
gnomAD v2: 2-113588114-CCAT-C
gnomAD v3: 2-112830537-CCAT-C
gnomAD v4: 2-112830537-CCAT-C
MyVariant Identifiers: chr2:g.113588115_113588117del (hg19) chr2:g.112830538_112830540del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830539_112830541del , CM000664.2:g.112830539_112830541del GRCh38
NC_000002.11:g.113588116_113588118del , CM000664.1:g.113588116_113588118del GRCh37
NC_000002.10:g.113304587_113304589del NCBI36
NG_008851.1:g.11240_11242del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.631_633del MANE Select ENSP00000263341.2:p.Met211del
ENST00000263341.6:c.631_633del ENSP00000263341.2:p.Met211del
ENST00000491056.5:n.1438_1440del
NM_000576.2:c.631_633del NP_000567.1:p.Met211del
XM_006712496.1:c.397_399del XP_006712559.1:p.Met133del
XM_017003988.2:c.538_540del XP_016859477.1:p.Met180del
NM_000576.3:c.631_633del MANE Select NP_000567.1:p.Met211del
Search 100 bp 5'
Search 100 bp 3'