Canonical Allele Identifier: CA1279917884
Gene: IL1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782617A= , CM000664.2:g.112782617A= GRCh38
NC_000002.11:g.113540194A= , CM000664.1:g.113540194A= GRCh37
NC_000002.10:g.113256665A= NCBI36
NG_008850.1:g.7778T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263339.4:c.96+99T= MANE Select ENSP00000263339.3:n.96+99T=
ENST00000263339.3:c.96+99T= ENSP00000263339.3:n.96+99T=
NM_000575.3:c.96+99T= NP_000566.3:n.96+99T=
NM_000575.4:c.96+99T= NP_000566.3:n.96+99T=
NM_000575.5:c.96+99T= MANE Select NP_000566.3:n.96+99T=
NM_001371554.1:c.96+99T= NP_001358483.1:n.96+99T=