Canonical Allele Identifier: CA382704631

Gene: APOA4

Linked Data

• dbSNP Id: rs758615168
• gnomAD v3: 11-116822668-T-G
• gnomAD v4: 11-116822668-T-G
• MyVariant Identifiers: chr11:g.116693384T>G (hg19) ; chr11:g.116822668T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116822668T>G , CM000673.2:g.116822668T>G	GRCh38
NC_000011.9:g.116693384T>G , CM000673.1:g.116693384T>G	GRCh37
NC_000011.8:g.116198594T>G	NCBI36
NG_012044.1:g.5628A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357780.5:c.167A>C MANE Select	ENSP00000350425.3:p.Gln56Pro
ENST00000357780.4:c.167A>C	ENSP00000350425.3:p.Gln56Pro
NM_000482.3:c.167A>C	NP_000473.2:p.Gln56Pro
NM_000482.4:c.167A>C MANE Select	NP_000473.2:p.Gln56Pro