Canonical Allele Identifier: CA2002755565
Gene: APOA4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822564G= , CM000673.2:g.116822564G= GRCh38
NC_000011.9:g.116693280G= , CM000673.1:g.116693280G= GRCh37
NC_000011.8:g.116198490G= NCBI36
NG_012044.1:g.5732C=

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.176+95C= MANE Select ENSP00000350425.3:n.176+95C=
ENST00000357780.4:c.176+95C= ENSP00000350425.3:n.176+95C=
NM_000482.3:c.176+95C= NP_000473.2:n.176+95C=
NM_000482.4:c.176+95C= MANE Select NP_000473.2:n.176+95C=
Search 100 bp 5'
Search 100 bp 3'