Canonical Allele Identifier: CA2660745817
Gene: IL1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112777865T>C , CM000664.2:g.112777865T>C GRCh38
NC_000002.11:g.113535442T>C , CM000664.1:g.113535442T>C GRCh37
NC_000002.10:g.113251913T>C NCBI36
NG_008850.1:g.12530A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263339.4:c.615+122A>G MANE Select ENSP00000263339.3:n.615+122A>G
ENST00000263339.3:c.615+122A>G ENSP00000263339.3:n.615+122A>G
NM_000575.3:c.615+122A>G NP_000566.3:n.615+122A>G
NM_000575.4:c.615+122A>G NP_000566.3:n.615+122A>G
NM_000575.5:c.615+122A>G MANE Select NP_000566.3:n.615+122A>G
NM_001371554.1:c.615+122A>G NP_001358483.1:n.615+122A>G