Canonical Allele Identifier: CA2603119343
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs2134218943
gnomAD v3: 11-116822578-T-C
gnomAD v4: 11-116822578-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822578T>C , CM000673.2:g.116822578T>C GRCh38
NC_000011.9:g.116693294T>C , CM000673.1:g.116693294T>C GRCh37
NC_000011.8:g.116198504T>C NCBI36
NG_012044.1:g.5718A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+81A>G MANE Select ENSP00000350425.3:n.176+81A>G
ENST00000357780.4:c.176+81A>G ENSP00000350425.3:n.176+81A>G
NM_000482.3:c.176+81A>G NP_000473.2:n.176+81A>G
NM_000482.4:c.176+81A>G MANE Select NP_000473.2:n.176+81A>G
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