Canonical Allele Identifier: CA476868546
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693491A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822775A>T , CM000673.2:g.116822775A>T GRCh38
NC_000011.9:g.116693491A>T , CM000673.1:g.116693491A>T GRCh37
NC_000011.8:g.116198701A>T NCBI36
NG_012044.1:g.5521T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.60T>A MANE Select ENSP00000350425.3:p.Ala20=
ENST00000357780.4:c.60T>A ENSP00000350425.3:p.Ala20=
NM_000482.3:c.60T>A NP_000473.2:p.Ala20=
NM_000482.4:c.60T>A MANE Select NP_000473.2:p.Ala20=
Search 100 bp 5'
Search 100 bp 3'