Canonical Allele Identifier: CA53661641

Gene: IL1A

Linked Data

• dbSNP Id: rs3783574
• gnomAD v2: 2-113540144-G-A
• gnomAD v3: 2-112782567-G-A
• gnomAD v4: 2-112782567-G-A
• MyVariant Identifiers: chr2:g.113540144G>A (hg19) ; chr2:g.112782567G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112782567G>A , CM000664.2:g.112782567G>A	GRCh38
NC_000002.11:g.113540144G>A , CM000664.1:g.113540144G>A	GRCh37
NC_000002.10:g.113256615G>A	NCBI36
NG_008850.1:g.7828C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263339.4:c.96+149C>T MANE Select	ENSP00000263339.3:n.96+149C>T
ENST00000263339.3:c.96+149C>T	ENSP00000263339.3:n.96+149C>T
NM_000575.3:c.96+149C>T	NP_000566.3:n.96+149C>T
NM_000575.4:c.96+149C>T	NP_000566.3:n.96+149C>T
NM_000575.5:c.96+149C>T MANE Select	NP_000566.3:n.96+149C>T
NM_001371554.1:c.96+149C>T	NP_001358483.1:n.96+149C>T