Canonical Allele Identifier: CA2660747024
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112831137-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831142del , CM000664.2:g.112831142del GRCh38
NC_000002.11:g.113588719del , CM000664.1:g.113588719del GRCh37
NC_000002.10:g.113305190del NCBI36
NG_008851.1:g.10642del

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.597+154del MANE Select ENSP00000263341.2:n.597+154del
ENST00000263341.6:c.597+154del ENSP00000263341.2:n.597+154del
ENST00000487639.1:n.652del
ENST00000491056.5:n.1404+154del
NM_000576.2:c.597+154del NP_000567.1:n.597+154del
XM_006712496.1:c.363+154del XP_006712559.1:n.363+154del
XM_017003988.2:c.504+154del XP_016859477.1:n.504+154del
NM_000576.3:c.597+154del MANE Select NP_000567.1:n.597+154del
Search 100 bp 5'
Search 100 bp 3'