Canonical Allele Identifier: CA476868418

Gene: APOA4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116822748C>G , CM000673.2:g.116822748C>G	GRCh38
NC_000011.9:g.116693464C>G , CM000673.1:g.116693464C>G	GRCh37
NC_000011.8:g.116198674C>G	NCBI36
NG_012044.1:g.5548G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357780.5:c.87G>C MANE Select	ENSP00000350425.3:p.Thr29=
ENST00000357780.4:c.87G>C	ENSP00000350425.3:p.Thr29=
NM_000482.3:c.87G>C	NP_000473.2:p.Thr29=
NM_000482.4:c.87G>C MANE Select	NP_000473.2:p.Thr29=