Canonical Allele Identifier: CA535228008
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1313028326
gnomAD v2: 2-113588714-T-A
gnomAD v3: 2-112831137-T-A
gnomAD v4: 2-112831137-T-A
MyVariant Identifiers: chr2:g.113588714T>A (hg19) chr2:g.112831137T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831137T>A , CM000664.2:g.112831137T>A GRCh38
NC_000002.11:g.113588714T>A , CM000664.1:g.113588714T>A GRCh37
NC_000002.10:g.113305185T>A NCBI36
NG_008851.1:g.10643A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.597+155A>T MANE Select ENSP00000263341.2:n.597+155A>T
ENST00000263341.6:c.597+155A>T ENSP00000263341.2:n.597+155A>T
ENST00000487639.1:n.653A>T
ENST00000491056.5:n.1404+155A>T
NM_000576.2:c.597+155A>T NP_000567.1:n.597+155A>T
XM_006712496.1:c.363+155A>T XP_006712559.1:n.363+155A>T
XM_017003988.2:c.504+155A>T XP_016859477.1:n.504+155A>T
NM_000576.3:c.597+155A>T MANE Select NP_000567.1:n.597+155A>T
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