Canonical Allele Identifier: CA382705073
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822752-G-A
MyVariant Identifiers: chr11:g.116693468G>A (hg19) chr11:g.116822752G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822752G>A , CM000673.2:g.116822752G>A GRCh38
NC_000011.9:g.116693468G>A , CM000673.1:g.116693468G>A GRCh37
NC_000011.8:g.116198678G>A NCBI36
NG_012044.1:g.5544C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.83C>T MANE Select ENSP00000350425.3:p.Ala28Val
ENST00000357780.4:c.83C>T ENSP00000350425.3:p.Ala28Val
NM_000482.3:c.83C>T NP_000473.2:p.Ala28Val
NM_000482.4:c.83C>T MANE Select NP_000473.2:p.Ala28Val
Search 100 bp 5'
Search 100 bp 3'