Canonical Allele Identifier: CA348286914
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113588110T>G (hg19) chr2:g.112830533T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830533T>G , CM000664.2:g.112830533T>G GRCh38
NC_000002.11:g.113588110T>G , CM000664.1:g.113588110T>G GRCh37
NC_000002.10:g.113304581T>G NCBI36
NG_008851.1:g.11247A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.638A>C MANE Select ENSP00000263341.2:p.Lys213Thr
ENST00000263341.6:c.638A>C ENSP00000263341.2:p.Lys213Thr
ENST00000491056.5:n.1445A>C
NM_000576.2:c.638A>C NP_000567.1:p.Lys213Thr
XM_006712496.1:c.404A>C XP_006712559.1:p.Lys135Thr
XM_017003988.2:c.545A>C XP_016859477.1:p.Lys182Thr
NM_000576.3:c.638A>C MANE Select NP_000567.1:p.Lys213Thr
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