Canonical Allele Identifier: CA1279917908
Gene: IL1A HGNC NCBI

Linked Data

dbSNP Id: rs1558771215

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782678G>C , CM000664.2:g.112782678G>C GRCh38
NC_000002.11:g.113540255G>C , CM000664.1:g.113540255G>C GRCh37
NC_000002.10:g.113256726G>C NCBI36
NG_008850.1:g.7717C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263339.4:c.96+38C>G MANE Select ENSP00000263339.3:n.96+38C>G
ENST00000263339.3:c.96+38C>G ENSP00000263339.3:n.96+38C>G
NM_000575.3:c.96+38C>G NP_000566.3:n.96+38C>G
NM_000575.4:c.96+38C>G NP_000566.3:n.96+38C>G
NM_000575.5:c.96+38C>G MANE Select NP_000566.3:n.96+38C>G
NM_001371554.1:c.96+38C>G NP_001358483.1:n.96+38C>G