Canonical Allele Identifier: CA348288268
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113590310T>C (hg19) chr2:g.112832733T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832733T>C , CM000664.2:g.112832733T>C GRCh38
NC_000002.11:g.113590310T>C , CM000664.1:g.113590310T>C GRCh37
NC_000002.10:g.113306781T>C NCBI36
NG_008851.1:g.9047A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.395A>G MANE Select ENSP00000263341.2:p.Lys132Arg
ENST00000263341.6:c.395A>G ENSP00000263341.2:p.Lys132Arg
ENST00000418817.5:c.395A>G ENSP00000407219.1:p.Lys132Arg
ENST00000487639.1:n.296A>G
ENST00000491056.5:n.1202A>G
NM_000576.2:c.395A>G NP_000567.1:p.Lys132Arg
XM_006712496.1:c.161A>G XP_006712559.1:p.Lys54Arg
XM_017003988.2:c.302A>G XP_016859477.1:p.Lys101Arg
NM_000576.3:c.395A>G MANE Select NP_000567.1:p.Lys132Arg
Search 100 bp 5'
Search 100 bp 3'