Canonical Allele Identifier: CA535596005
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1218181150
gnomAD v2: 2-113588113-TCCATCTTC-T
gnomAD v3: 2-112830536-TCCATCTTC-T
gnomAD v4: 2-112830536-TCCATCTTC-T
MyVariant Identifiers: chr2:g.113588114_113588121del (hg19) chr2:g.112830537_112830544del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830537_112830544del , CM000664.2:g.112830537_112830544del GRCh38
NC_000002.11:g.113588114_113588121del , CM000664.1:g.113588114_113588121del GRCh37
NC_000002.10:g.113304585_113304592del NCBI36
NG_008851.1:g.11236_11243del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.627_634del MANE Select ENSP00000263341.2:p.Met211AlafsTer11
ENST00000263341.6:c.627_634del ENSP00000263341.2:p.Met211AlafsTer11
ENST00000491056.5:n.1434_1441del
NM_000576.2:c.627_634del NP_000567.1:p.Met211AlafsTer11
XM_006712496.1:c.393_400del XP_006712559.1:p.Met133AlafsTer11
XM_017003988.2:c.534_541del XP_016859477.1:p.Met180AlafsTer11
NM_000576.3:c.627_634del MANE Select NP_000567.1:p.Met211AlafsTer11
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