Canonical Allele Identifier: CA53661661
Gene: IL1A HGNC NCBI

Linked Data

dbSNP Id: rs1037701461
MyVariant Identifiers: chr2:g.113540194A>T (hg19) chr2:g.112782617A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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