Canonical Allele Identifier: CA2577073788
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112830630-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830630A>T , CM000664.2:g.112830630A>T GRCh38
NC_000002.11:g.113588207A>T , CM000664.1:g.113588207A>T GRCh37
NC_000002.10:g.113304678A>T NCBI36
NG_008851.1:g.11150T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-57T>A MANE Select ENSP00000263341.2:n.598-57T>A
ENST00000263341.6:c.598-57T>A ENSP00000263341.2:n.598-57T>A
ENST00000491056.5:n.1405-57T>A
NM_000576.2:c.598-57T>A NP_000567.1:n.598-57T>A
XM_006712496.1:c.364-57T>A XP_006712559.1:n.364-57T>A
XM_017003988.2:c.505-57T>A XP_016859477.1:n.505-57T>A
NM_000576.3:c.598-57T>A MANE Select NP_000567.1:n.598-57T>A
Search 100 bp 5'
Search 100 bp 3'