Canonical Allele Identifier: CA2660747766
Gene: IL1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782649dup , CM000664.2:g.112782649dup GRCh38
NC_000002.11:g.113540226dup , CM000664.1:g.113540226dup GRCh37
NC_000002.10:g.113256697dup NCBI36
NG_008850.1:g.7747dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263339.4:c.96+68dup MANE Select ENSP00000263339.3:n.96+68dup
ENST00000263339.3:c.96+68dup ENSP00000263339.3:n.96+68dup
NM_000575.3:c.96+68dup NP_000566.3:n.96+68dup
NM_000575.4:c.96+68dup NP_000566.3:n.96+68dup
NM_000575.5:c.96+68dup MANE Select NP_000566.3:n.96+68dup
NM_001371554.1:c.96+68dup NP_001358483.1:n.96+68dup