Canonical Allele Identifier: CA348288027
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113590239C>T (hg19) chr2:g.112832662C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832662C>T , CM000664.2:g.112832662C>T GRCh38
NC_000002.11:g.113590239C>T , CM000664.1:g.113590239C>T GRCh37
NC_000002.10:g.113306710C>T NCBI36
NG_008851.1:g.9118G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466G>A MANE Select ENSP00000263341.2:p.Val156Met
ENST00000263341.6:c.466G>A ENSP00000263341.2:p.Val156Met
ENST00000487639.1:n.367G>A
ENST00000491056.5:n.1273G>A
NM_000576.2:c.466G>A NP_000567.1:p.Val156Met
XM_006712496.1:c.232G>A XP_006712559.1:p.Val78Met
XM_017003988.2:c.373G>A XP_016859477.1:p.Val125Met
NM_000576.3:c.466G>A MANE Select NP_000567.1:p.Val156Met
Search 100 bp 5'
Search 100 bp 3'