Canonical Allele Identifier: CA535224876

Gene: IL1A

Linked Data

• dbSNP Id: rs1344196999
• gnomAD v2: 2-113540114-C-A
• gnomAD v3: 2-112782537-C-A
• gnomAD v4: 2-112782537-C-A
• MyVariant Identifiers: chr2:g.113540114C>A (hg19) ; chr2:g.112782537C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112782537C>A , CM000664.2:g.112782537C>A	GRCh38
NC_000002.11:g.113540114C>A , CM000664.1:g.113540114C>A	GRCh37
NC_000002.10:g.113256585C>A	NCBI36
NG_008850.1:g.7858G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263339.4:c.96+179G>T MANE Select	ENSP00000263339.3:n.96+179G>T
ENST00000263339.3:c.96+179G>T	ENSP00000263339.3:n.96+179G>T
NM_000575.3:c.96+179G>T	NP_000566.3:n.96+179G>T
NM_000575.4:c.96+179G>T	NP_000566.3:n.96+179G>T
NM_000575.5:c.96+179G>T MANE Select	NP_000566.3:n.96+179G>T
NM_001371554.1:c.96+179G>T	NP_001358483.1:n.96+179G>T