Canonical Allele Identifier: CA476868423
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693470C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822754C>G , CM000673.2:g.116822754C>G GRCh38
NC_000011.9:g.116693470C>G , CM000673.1:g.116693470C>G GRCh37
NC_000011.8:g.116198680C>G NCBI36
NG_012044.1:g.5542G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.81G>C MANE Select ENSP00000350425.3:p.Val27=
ENST00000357780.4:c.81G>C ENSP00000350425.3:p.Val27=
NM_000482.3:c.81G>C NP_000473.2:p.Val27=
NM_000482.4:c.81G>C MANE Select NP_000473.2:p.Val27=
Search 100 bp 5'
Search 100 bp 3'