Canonical Allele Identifier: CA15176763
Gene: IL1A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1609682

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_000575.3:c.96+88C>A VV NP_000566.3:p.=
NM_000575.4:c.96+88C>A VV NP_000566.3:p.=
ENST00000263339.3:c.96+88C>A ENSP00000263339.3:p.=