Canonical Allele Identifier: CA6289537
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs750526475
ExAC: 11:116693463 C / T
gnomAD v2: 11-116693463-C-T
MyVariant Identifiers: chr11:g.116693463C>T (hg19) chr11:g.116822747C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822747C>T , CM000673.2:g.116822747C>T GRCh38
NC_000011.9:g.116693463C>T , CM000673.1:g.116693463C>T GRCh37
NC_000011.8:g.116198673C>T NCBI36
NG_012044.1:g.5549G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.88G>A MANE Select ENSP00000350425.3:p.Val30Met
ENST00000357780.4:c.88G>A ENSP00000350425.3:p.Val30Met
NM_000482.3:c.88G>A NP_000473.2:p.Val30Met
NM_000482.4:c.88G>A MANE Select NP_000473.2:p.Val30Met
Search 100 bp 5'
Search 100 bp 3'