Canonical Allele Identifier: CA2002755697
Gene: APOA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822858A= , CM000673.2:g.116822858A= GRCh38
NC_000011.9:g.116693574A= , CM000673.1:g.116693574A= GRCh37
NC_000011.8:g.116198784A= NCBI36
NG_012044.1:g.5438T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.50-73T= MANE Select ENSP00000350425.3:n.50-73T=
ENST00000357780.4:c.50-73T= ENSP00000350425.3:n.50-73T=
NM_000482.3:c.50-73T= NP_000473.2:n.50-73T=
NM_000482.4:c.50-73T= MANE Select NP_000473.2:n.50-73T=
Search 100 bp 5'
Search 100 bp 3'