Canonical Allele Identifier: CA428299459
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112832735-T-C
MyVariant Identifiers: chr2:g.113590312T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832735T>C , CM000664.2:g.112832735T>C GRCh38
NC_000002.11:g.113590312T>C , CM000664.1:g.113590312T>C GRCh37
NC_000002.10:g.113306783T>C NCBI36
NG_008851.1:g.9045A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.393A>G MANE Select ENSP00000263341.2:p.Gln131=
ENST00000263341.6:c.393A>G ENSP00000263341.2:p.Gln131=
ENST00000418817.5:c.393A>G ENSP00000407219.1:p.Gln131=
ENST00000487639.1:n.294A>G
ENST00000491056.5:n.1200A>G
NM_000576.2:c.393A>G NP_000567.1:p.Gln131=
XM_006712496.1:c.159A>G XP_006712559.1:p.Gln53=
XM_017003988.2:c.300A>G XP_016859477.1:p.Gln100=
NM_000576.3:c.393A>G MANE Select NP_000567.1:p.Gln131=
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