Canonical Allele Identifier: CA348288277
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113590313T>C (hg19) chr2:g.112832736T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832736T>C , CM000664.2:g.112832736T>C GRCh38
NC_000002.11:g.113590313T>C , CM000664.1:g.113590313T>C GRCh37
NC_000002.10:g.113306784T>C NCBI36
NG_008851.1:g.9044A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.392A>G MANE Select ENSP00000263341.2:p.Gln131Arg
ENST00000263341.6:c.392A>G ENSP00000263341.2:p.Gln131Arg
ENST00000418817.5:c.392A>G ENSP00000407219.1:p.Gln131Arg
ENST00000487639.1:n.293A>G
ENST00000491056.5:n.1199A>G
NM_000576.2:c.392A>G NP_000567.1:p.Gln131Arg
XM_006712496.1:c.158A>G XP_006712559.1:p.Gln53Arg
XM_017003988.2:c.299A>G XP_016859477.1:p.Gln100Arg
NM_000576.3:c.392A>G MANE Select NP_000567.1:p.Gln131Arg
Search 100 bp 5'
Search 100 bp 3'