Canonical Allele Identifier: CA2002755568
Gene: APOA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822572C= , CM000673.2:g.116822572C= GRCh38
NC_000011.9:g.116693288C= , CM000673.1:g.116693288C= GRCh37
NC_000011.8:g.116198498C= NCBI36
NG_012044.1:g.5724G=

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.176+87G= MANE Select ENSP00000350425.3:n.176+87G=
ENST00000357780.4:c.176+87G= ENSP00000350425.3:n.176+87G=
NM_000482.3:c.176+87G= NP_000473.2:n.176+87G=
NM_000482.4:c.176+87G= MANE Select NP_000473.2:n.176+87G=
Search 100 bp 5'
Search 100 bp 3'