Canonical Allele Identifier: CA2839239729
Gene: APOA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822831G>T , CM000673.2:g.116822831G>T GRCh38
NC_000011.9:g.116693547G>T , CM000673.1:g.116693547G>T GRCh37
NC_000011.8:g.116198757G>T NCBI36
NG_012044.1:g.5465C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.50-46C>A MANE Select ENSP00000350425.3:n.50-46C>A
ENST00000357780.4:c.50-46C>A ENSP00000350425.3:n.50-46C>A
NM_000482.3:c.50-46C>A NP_000473.2:n.50-46C>A
NM_000482.4:c.50-46C>A MANE Select NP_000473.2:n.50-46C>A
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