Canonical Allele Identifier: CA6289551
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs777021006
ExAC: 11:116693543 G / A
gnomAD v2: 11-116693543-G-A
gnomAD v3: 11-116822827-G-A
gnomAD v4: 11-116822827-G-A
MyVariant Identifiers: chr11:g.116693543G>A (hg19) chr11:g.116822827G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822827G>A , CM000673.2:g.116822827G>A GRCh38
NC_000011.9:g.116693543G>A , CM000673.1:g.116693543G>A GRCh37
NC_000011.8:g.116198753G>A NCBI36
NG_012044.1:g.5469C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.50-42C>T MANE Select ENSP00000350425.3:n.50-42C>T
ENST00000357780.4:c.50-42C>T ENSP00000350425.3:n.50-42C>T
NM_000482.3:c.50-42C>T NP_000473.2:n.50-42C>T
NM_000482.4:c.50-42C>T MANE Select NP_000473.2:n.50-42C>T
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