Canonical Allele Identifier: CA2002755642
Gene: APOA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822718G= , CM000673.2:g.116822718G= GRCh38
NC_000011.9:g.116693434G= , CM000673.1:g.116693434G= GRCh37
NC_000011.8:g.116198644G= NCBI36
NG_012044.1:g.5578C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.117C= MANE Select ENSP00000350425.3:p.Ser39=
ENST00000357780.4:c.117C= ENSP00000350425.3:p.Ser39=
NM_000482.3:c.117C= NP_000473.2:p.Ser39=
NM_000482.4:c.117C= MANE Select NP_000473.2:p.Ser39=
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