Canonical Allele Identifier: CA348287032
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113588129G>T (hg19) chr2:g.112830552G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830552G>T , CM000664.2:g.112830552G>T GRCh38
NC_000002.11:g.113588129G>T , CM000664.1:g.113588129G>T GRCh37
NC_000002.10:g.113304600G>T NCBI36
NG_008851.1:g.11228C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.619C>A MANE Select ENSP00000263341.2:p.Pro207Thr
ENST00000263341.6:c.619C>A ENSP00000263341.2:p.Pro207Thr
ENST00000491056.5:n.1426C>A
NM_000576.2:c.619C>A NP_000567.1:p.Pro207Thr
XM_006712496.1:c.385C>A XP_006712559.1:p.Pro129Thr
XM_017003988.2:c.526C>A XP_016859477.1:p.Pro176Thr
NM_000576.3:c.619C>A MANE Select NP_000567.1:p.Pro207Thr
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