Canonical Allele Identifier: CA1279917890
Gene: IL1A HGNC NCBI

Linked Data

dbSNP Id: rs1681232176
gnomAD v4: 2-112782632-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782632A>G , CM000664.2:g.112782632A>G GRCh38
NC_000002.11:g.113540209A>G , CM000664.1:g.113540209A>G GRCh37
NC_000002.10:g.113256680A>G NCBI36
NG_008850.1:g.7763T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263339.4:c.96+84T>C MANE Select ENSP00000263339.3:n.96+84T>C
ENST00000263339.3:c.96+84T>C ENSP00000263339.3:n.96+84T>C
NM_000575.3:c.96+84T>C NP_000566.3:n.96+84T>C
NM_000575.4:c.96+84T>C NP_000566.3:n.96+84T>C
NM_000575.5:c.96+84T>C MANE Select NP_000566.3:n.96+84T>C
NM_001371554.1:c.96+84T>C NP_001358483.1:n.96+84T>C
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