Canonical Allele Identifier: CA2002755569
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs1941339260
gnomAD v4: 11-116822572-C-A
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+87G>T MANE Select ENSP00000350425.3:n.176+87G>T
ENST00000357780.4:c.176+87G>T ENSP00000350425.3:n.176+87G>T
NM_000482.3:c.176+87G>T NP_000473.2:n.176+87G>T
NM_000482.4:c.176+87G>T MANE Select NP_000473.2:n.176+87G>T
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