Canonical Allele Identifier: CA53698023
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs753947473
gnomAD v2: 2-113590234-T-C
gnomAD v4: 2-112832657-T-C
MyVariant Identifiers: chr2:g.113590234T>C (hg19) chr2:g.112832657T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832657T>C , CM000664.2:g.112832657T>C GRCh38
NC_000002.11:g.113590234T>C , CM000664.1:g.113590234T>C GRCh37
NC_000002.10:g.113306705T>C NCBI36
NG_008851.1:g.9123A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+5A>G MANE Select ENSP00000263341.2:n.466+5A>G
ENST00000263341.6:c.466+5A>G ENSP00000263341.2:n.466+5A>G
ENST00000487639.1:n.367+5A>G
ENST00000491056.5:n.1273+5A>G
NM_000576.2:c.466+5A>G NP_000567.1:n.466+5A>G
XM_006712496.1:c.232+5A>G XP_006712559.1:n.232+5A>G
XM_017003988.2:c.373+5A>G XP_016859477.1:n.373+5A>G
NM_000576.3:c.466+5A>G MANE Select NP_000567.1:n.466+5A>G
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