Canonical Allele Identifier: CA654624817
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs1591322965
gnomAD v4: 11-116822552-T-G
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+107A>C MANE Select ENSP00000350425.3:n.176+107A>C
ENST00000357780.4:c.176+107A>C ENSP00000350425.3:n.176+107A>C
NM_000482.3:c.176+107A>C NP_000473.2:n.176+107A>C
NM_000482.4:c.176+107A>C MANE Select NP_000473.2:n.176+107A>C
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