Canonical Allele Identifier: CA2002755652
Gene: APOA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822749G= , CM000673.2:g.116822749G= GRCh38
NC_000011.9:g.116693465G= , CM000673.1:g.116693465G= GRCh37
NC_000011.8:g.116198675G= NCBI36
NG_012044.1:g.5547C=

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.86C= MANE Select ENSP00000350425.3:p.Thr29=
ENST00000357780.4:c.86C= ENSP00000350425.3:p.Thr29=
NM_000482.3:c.86C= NP_000473.2:p.Thr29=
NM_000482.4:c.86C= MANE Select NP_000473.2:p.Thr29=