Canonical Allele Identifier: CA2002755572
Gene: APOA4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822583A= , CM000673.2:g.116822583A= GRCh38
NC_000011.9:g.116693299A= , CM000673.1:g.116693299A= GRCh37
NC_000011.8:g.116198509A= NCBI36
NG_012044.1:g.5713T=

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.176+76T= MANE Select ENSP00000350425.3:n.176+76T=
ENST00000357780.4:c.176+76T= ENSP00000350425.3:n.176+76T=
NM_000482.3:c.176+76T= NP_000473.2:n.176+76T=
NM_000482.4:c.176+76T= MANE Select NP_000473.2:n.176+76T=
Search 100 bp 5'
Search 100 bp 3'