Canonical Allele Identifier: CA348287033
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113588130G>C (hg19) chr2:g.112830553G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830553G>C , CM000664.2:g.112830553G>C GRCh38
NC_000002.11:g.113588130G>C , CM000664.1:g.113588130G>C GRCh37
NC_000002.10:g.113304601G>C NCBI36
NG_008851.1:g.11227C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.618C>G MANE Select ENSP00000263341.2:p.Tyr206Ter
ENST00000263341.6:c.618C>G ENSP00000263341.2:p.Tyr206Ter
ENST00000491056.5:n.1425C>G
NM_000576.2:c.618C>G NP_000567.1:p.Tyr206Ter
XM_006712496.1:c.384C>G XP_006712559.1:p.Tyr128Ter
XM_017003988.2:c.525C>G XP_016859477.1:p.Tyr175Ter
NM_000576.3:c.618C>G MANE Select NP_000567.1:p.Tyr206Ter
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