Canonical Allele Identifier: CA2616109650
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822554-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822554G>C , CM000673.2:g.116822554G>C GRCh38
NC_000011.9:g.116693270G>C , CM000673.1:g.116693270G>C GRCh37
NC_000011.8:g.116198480G>C NCBI36
NG_012044.1:g.5742C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+105C>G MANE Select ENSP00000350425.3:n.176+105C>G
ENST00000357780.4:c.176+105C>G ENSP00000350425.3:n.176+105C>G
NM_000482.3:c.176+105C>G NP_000473.2:n.176+105C>G
NM_000482.4:c.176+105C>G MANE Select NP_000473.2:n.176+105C>G
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