Canonical Allele Identifier: CA428299486
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113590318T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832741T>A , CM000664.2:g.112832741T>A GRCh38
NC_000002.11:g.113590318T>A , CM000664.1:g.113590318T>A GRCh37
NC_000002.10:g.113306789T>A NCBI36
NG_008851.1:g.9039A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.387A>T MANE Select ENSP00000263341.2:p.Ser129=
ENST00000263341.6:c.387A>T ENSP00000263341.2:p.Ser129=
ENST00000418817.5:c.387A>T ENSP00000407219.1:p.Ser129=
ENST00000487639.1:n.288A>T
ENST00000491056.5:n.1194A>T
NM_000576.2:c.387A>T NP_000567.1:p.Ser129=
XM_006712496.1:c.153A>T XP_006712559.1:p.Ser51=
XM_017003988.2:c.294A>T XP_016859477.1:p.Ser98=
NM_000576.3:c.387A>T MANE Select NP_000567.1:p.Ser129=
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