Canonical Allele Identifier: CA2616109664
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822584-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822584A>G , CM000673.2:g.116822584A>G GRCh38
NC_000011.9:g.116693300A>G , CM000673.1:g.116693300A>G GRCh37
NC_000011.8:g.116198510A>G NCBI36
NG_012044.1:g.5712T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.176+75T>C MANE Select ENSP00000350425.3:n.176+75T>C
ENST00000357780.4:c.176+75T>C ENSP00000350425.3:n.176+75T>C
NM_000482.3:c.176+75T>C NP_000473.2:n.176+75T>C
NM_000482.4:c.176+75T>C MANE Select NP_000473.2:n.176+75T>C
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