Canonical Allele Identifier: CA6289540
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs752498966
ExAC: 11:116693469 C / G
gnomAD v2: 11-116693469-C-G
gnomAD v4: 11-116822753-C-G
MyVariant Identifiers: chr11:g.116693469C>G (hg19) chr11:g.116822753C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822753C>G , CM000673.2:g.116822753C>G GRCh38
NC_000011.9:g.116693469C>G , CM000673.1:g.116693469C>G GRCh37
NC_000011.8:g.116198679C>G NCBI36
NG_012044.1:g.5543G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.82G>C MANE Select ENSP00000350425.3:p.Ala28Pro
ENST00000357780.4:c.82G>C ENSP00000350425.3:p.Ala28Pro
NM_000482.3:c.82G>C NP_000473.2:p.Ala28Pro
NM_000482.4:c.82G>C MANE Select NP_000473.2:p.Ala28Pro
Search 100 bp 5'
Search 100 bp 3'