Canonical Allele Identifier: CA535596011
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1196169738
gnomAD v2: 2-113588134-T-TG
gnomAD v3: 2-112830557-T-TG
gnomAD v4: 2-112830557-T-TG
MyVariant Identifiers: chr2:g.113588134_113588135insG (hg19) chr2:g.112830557_112830558insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830557_112830558insG , CM000664.2:g.112830557_112830558insG GRCh38
NC_000002.11:g.113588134_113588135insG , CM000664.1:g.113588134_113588135insG GRCh37
NC_000002.10:g.113304605_113304606insG NCBI36
NG_008851.1:g.11222_11223insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.613_614insC MANE Select ENSP00000263341.2:p.Asn205ThrfsTer20
ENST00000263341.6:c.613_614insC ENSP00000263341.2:p.Asn205ThrfsTer20
ENST00000491056.5:n.1420_1421insC
NM_000576.2:c.613_614insC NP_000567.1:p.Asn205ThrfsTer20
XM_006712496.1:c.379_380insC XP_006712559.1:p.Asn127ThrfsTer20
XM_017003988.2:c.520_521insC XP_016859477.1:p.Asn174ThrfsTer20
NM_000576.3:c.613_614insC MANE Select NP_000567.1:p.Asn205ThrfsTer20
Search 100 bp 5'
Search 100 bp 3'