Canonical Allele Identifier: CA2660747779
Gene: IL1A HGNC NCBI

Linked Data

gnomAD v4: 2-112782675-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782675T>C , CM000664.2:g.112782675T>C GRCh38
NC_000002.11:g.113540252T>C , CM000664.1:g.113540252T>C GRCh37
NC_000002.10:g.113256723T>C NCBI36
NG_008850.1:g.7720A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263339.4:c.96+41A>G MANE Select ENSP00000263339.3:n.96+41A>G
ENST00000263339.3:c.96+41A>G ENSP00000263339.3:n.96+41A>G
NM_000575.3:c.96+41A>G NP_000566.3:n.96+41A>G
NM_000575.4:c.96+41A>G NP_000566.3:n.96+41A>G
NM_000575.5:c.96+41A>G MANE Select NP_000566.3:n.96+41A>G
NM_001371554.1:c.96+41A>G NP_001358483.1:n.96+41A>G
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