Canonical Allele Identifier: CA382706463
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693478C>A (hg19) chr11:g.116822762C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822762C>A , CM000673.2:g.116822762C>A GRCh38
NC_000011.9:g.116693478C>A , CM000673.1:g.116693478C>A GRCh37
NC_000011.8:g.116198688C>A NCBI36
NG_012044.1:g.5534G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.73G>T MANE Select ENSP00000350425.3:p.Asp25Tyr
ENST00000357780.4:c.73G>T ENSP00000350425.3:p.Asp25Tyr
NM_000482.3:c.73G>T NP_000473.2:p.Asp25Tyr
NM_000482.4:c.73G>T MANE Select NP_000473.2:p.Asp25Tyr
Search 100 bp 5'
Search 100 bp 3'