Canonical Allele Identifier: CA1279917878
Gene: IL1A HGNC NCBI

Linked Data

dbSNP Id: rs1681231657
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782608G>A , CM000664.2:g.112782608G>A GRCh38
NC_000002.11:g.113540185G>A , CM000664.1:g.113540185G>A GRCh37
NC_000002.10:g.113256656G>A NCBI36
NG_008850.1:g.7787C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263339.4:c.96+108C>T MANE Select ENSP00000263339.3:n.96+108C>T
ENST00000263339.3:c.96+108C>T ENSP00000263339.3:n.96+108C>T
NM_000575.3:c.96+108C>T NP_000566.3:n.96+108C>T
NM_000575.4:c.96+108C>T NP_000566.3:n.96+108C>T
NM_000575.5:c.96+108C>T MANE Select NP_000566.3:n.96+108C>T
NM_001371554.1:c.96+108C>T NP_001358483.1:n.96+108C>T
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Search 100 bp 3'