Canonical Allele Identifier: CA1279917888
Gene: IL1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782628G= , CM000664.2:g.112782628G= GRCh38
NC_000002.11:g.113540205G= , CM000664.1:g.113540205G= GRCh37
NC_000002.10:g.113256676G= NCBI36
NG_008850.1:g.7767C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263339.4:c.96+88C= MANE Select ENSP00000263339.3:n.96+88C=
ENST00000263339.3:c.96+88C= ENSP00000263339.3:n.96+88C=
NM_000575.3:c.96+88C= NP_000566.3:n.96+88C=
NM_000575.4:c.96+88C= NP_000566.3:n.96+88C=
NM_000575.5:c.96+88C= MANE Select NP_000566.3:n.96+88C=
NM_001371554.1:c.96+88C= NP_001358483.1:n.96+88C=
Search 100 bp 5'
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