Canonical Allele Identifier: CA1279917837
Gene: IL1A HGNC NCBI

Linked Data

dbSNP Id: rs1681229448
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782518G>T , CM000664.2:g.112782518G>T GRCh38
NC_000002.11:g.113540095G>T , CM000664.1:g.113540095G>T GRCh37
NC_000002.10:g.113256566G>T NCBI36
NG_008850.1:g.7877C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263339.4:c.96+198C>A MANE Select ENSP00000263339.3:n.96+198C>A
ENST00000263339.3:c.96+198C>A ENSP00000263339.3:n.96+198C>A
NM_000575.3:c.96+198C>A NP_000566.3:n.96+198C>A
NM_000575.4:c.96+198C>A NP_000566.3:n.96+198C>A
NM_000575.5:c.96+198C>A MANE Select NP_000566.3:n.96+198C>A
NM_001371554.1:c.96+198C>A NP_001358483.1:n.96+198C>A
Search 100 bp 5'
Search 100 bp 3'