Canonical Allele Identifier: CA2700333944
Gene: IL1A HGNC NCBI

Linked Data

dbSNP Id: rs2104907018

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112777817A>C , CM000664.2:g.112777817A>C GRCh38
NC_000002.11:g.113535394A>C , CM000664.1:g.113535394A>C GRCh37
NC_000002.10:g.113251865A>C NCBI36
NG_008850.1:g.12578T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263339.4:c.615+170T>G MANE Select ENSP00000263339.3:n.615+170T>G
ENST00000263339.3:c.615+170T>G ENSP00000263339.3:n.615+170T>G
NM_000575.3:c.615+170T>G NP_000566.3:n.615+170T>G
NM_000575.4:c.615+170T>G NP_000566.3:n.615+170T>G
NM_000575.5:c.615+170T>G MANE Select NP_000566.3:n.615+170T>G
NM_001371554.1:c.615+170T>G NP_001358483.1:n.615+170T>G