Canonical Allele Identifier: CA2002755559
Gene: APOA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822552T= , CM000673.2:g.116822552T= GRCh38
NC_000011.9:g.116693268T= , CM000673.1:g.116693268T= GRCh37
NC_000011.8:g.116198478T= NCBI36
NG_012044.1:g.5744A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+107A= MANE Select ENSP00000350425.3:n.176+107A=
ENST00000357780.4:c.176+107A= ENSP00000350425.3:n.176+107A=
NM_000482.3:c.176+107A= NP_000473.2:n.176+107A=
NM_000482.4:c.176+107A= MANE Select NP_000473.2:n.176+107A=
Search 100 bp 5'
Search 100 bp 3'