Canonical Allele Identifier: CA348287091
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113588146A>C (hg19) chr2:g.112830569A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830569A>C , CM000664.2:g.112830569A>C GRCh38
NC_000002.11:g.113588146A>C , CM000664.1:g.113588146A>C GRCh37
NC_000002.10:g.113304617A>C NCBI36
NG_008851.1:g.11211T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.602T>G MANE Select ENSP00000263341.2:p.Val201Gly
ENST00000263341.6:c.602T>G ENSP00000263341.2:p.Val201Gly
ENST00000491056.5:n.1409T>G
NM_000576.2:c.602T>G NP_000567.1:p.Val201Gly
XM_006712496.1:c.368T>G XP_006712559.1:p.Val123Gly
XM_017003988.2:c.509T>G XP_016859477.1:p.Val170Gly
NM_000576.3:c.602T>G MANE Select NP_000567.1:p.Val201Gly
Search 100 bp 5'
Search 100 bp 3'