Canonical Allele Identifier: CA755254979
Gene: IL1A HGNC NCBI

Linked Data

dbSNP Id: rs1337926450
gnomAD v3: 2-112777790-C-T
gnomAD v4: 2-112777790-C-T
MyVariant Identifiers: chr2:g.113535367C>T (hg19) chr2:g.112777790C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112777790C>T , CM000664.2:g.112777790C>T GRCh38
NC_000002.11:g.113535367C>T , CM000664.1:g.113535367C>T GRCh37
NC_000002.10:g.113251838C>T NCBI36
NG_008850.1:g.12605G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263339.4:c.615+197G>A MANE Select ENSP00000263339.3:n.615+197G>A
ENST00000263339.3:c.615+197G>A ENSP00000263339.3:n.615+197G>A
NM_000575.3:c.615+197G>A NP_000566.3:n.615+197G>A
NM_000575.4:c.615+197G>A NP_000566.3:n.615+197G>A
NM_000575.5:c.615+197G>A MANE Select NP_000566.3:n.615+197G>A
NM_001371554.1:c.615+197G>A NP_001358483.1:n.615+197G>A
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