Canonical Allele Identifier: CA2002755571
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs1941339279
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822581C>T , CM000673.2:g.116822581C>T GRCh38
NC_000011.9:g.116693297C>T , CM000673.1:g.116693297C>T GRCh37
NC_000011.8:g.116198507C>T NCBI36
NG_012044.1:g.5715G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+78G>A MANE Select ENSP00000350425.3:n.176+78G>A
ENST00000357780.4:c.176+78G>A ENSP00000350425.3:n.176+78G>A
NM_000482.3:c.176+78G>A NP_000473.2:n.176+78G>A
NM_000482.4:c.176+78G>A MANE Select NP_000473.2:n.176+78G>A
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