Canonical Allele Identifier: CA535595904
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs879633470
gnomAD v2: 2-113588378-A-AT
gnomAD v3: 2-112830801-A-AT
gnomAD v4: 2-112830801-A-AT
MyVariant Identifiers: chr2:g.113588379_113588380insT (hg19) chr2:g.113588378_113588379insT (hg19) chr2:g.112830802_112830803insT (hg38) chr2:g.112830801_112830802insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830813dup , CM000664.2:g.112830813dup GRCh38
NC_000002.11:g.113588390dup , CM000664.1:g.113588390dup GRCh37
NC_000002.10:g.113304861dup NCBI36
NG_008851.1:g.10978dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-229dup MANE Select ENSP00000263341.2:n.598-229dup
ENST00000263341.6:c.598-229dup ENSP00000263341.2:n.598-229dup
ENST00000491056.5:n.1405-229dup
NM_000576.2:c.598-229dup NP_000567.1:n.598-229dup
XM_006712496.1:c.364-229dup XP_006712559.1:n.364-229dup
XM_017003988.2:c.505-229dup XP_016859477.1:n.505-229dup
NM_000576.3:c.598-229dup MANE Select NP_000567.1:n.598-229dup
Search 100 bp 5'
Search 100 bp 3'