Canonical Allele Identifier: CA2616109698
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822832-G-GC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822836dup , CM000673.2:g.116822836dup GRCh38
NC_000011.9:g.116693552dup , CM000673.1:g.116693552dup GRCh37
NC_000011.8:g.116198762dup NCBI36
NG_012044.1:g.5463dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.50-48dup MANE Select ENSP00000350425.3:n.50-48dup
ENST00000357780.4:c.50-48dup ENSP00000350425.3:n.50-48dup
NM_000482.3:c.50-48dup NP_000473.2:n.50-48dup
NM_000482.4:c.50-48dup MANE Select NP_000473.2:n.50-48dup
Search 100 bp 5'
Search 100 bp 3'