Canonical Allele Identifier: CA428298866
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs953191369
gnomAD v3: 2-112830531-G-T
gnomAD v4: 2-112830531-G-T
MyVariant Identifiers: chr2:g.113588108G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830531G>T , CM000664.2:g.112830531G>T GRCh38
NC_000002.11:g.113588108G>T , CM000664.1:g.113588108G>T GRCh37
NC_000002.10:g.113304579G>T NCBI36
NG_008851.1:g.11249C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.640C>A MANE Select ENSP00000263341.2:p.Arg214=
ENST00000263341.6:c.640C>A ENSP00000263341.2:p.Arg214=
ENST00000491056.5:n.1447C>A
NM_000576.2:c.640C>A NP_000567.1:p.Arg214=
XM_006712496.1:c.406C>A XP_006712559.1:p.Arg136=
XM_017003988.2:c.547C>A XP_016859477.1:p.Arg183=
NM_000576.3:c.640C>A MANE Select NP_000567.1:p.Arg214=
Search 100 bp 5'
Search 100 bp 3'