Canonical Allele Identifier: CA382704666
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693393T>G (hg19) chr11:g.116822677T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822677T>G , CM000673.2:g.116822677T>G GRCh38
NC_000011.9:g.116693393T>G , CM000673.1:g.116693393T>G GRCh37
NC_000011.8:g.116198603T>G NCBI36
NG_012044.1:g.5619A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.158A>C MANE Select ENSP00000350425.3:p.Glu53Ala
ENST00000357780.4:c.158A>C ENSP00000350425.3:p.Glu53Ala
NM_000482.3:c.158A>C NP_000473.2:p.Glu53Ala
NM_000482.4:c.158A>C MANE Select NP_000473.2:p.Glu53Ala
Search 100 bp 5'
Search 100 bp 3'