Canonical Allele Identifier: CA53661637

Gene: IL1A

Linked Data

• dbSNP Id: rs923533723
• MyVariant Identifiers: chr2:g.113540124A>G (hg19) ; chr2:g.112782547A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112782547A>G , CM000664.2:g.112782547A>G	GRCh38
NC_000002.11:g.113540124A>G , CM000664.1:g.113540124A>G	GRCh37
NC_000002.10:g.113256595A>G	NCBI36
NG_008850.1:g.7848T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263339.4:c.96+169T>C MANE Select	ENSP00000263339.3:n.96+169T>C
ENST00000263339.3:c.96+169T>C	ENSP00000263339.3:n.96+169T>C
NM_000575.3:c.96+169T>C	NP_000566.3:n.96+169T>C
NM_000575.4:c.96+169T>C	NP_000566.3:n.96+169T>C
NM_000575.5:c.96+169T>C MANE Select	NP_000566.3:n.96+169T>C
NM_001371554.1:c.96+169T>C	NP_001358483.1:n.96+169T>C