Canonical Allele Identifier: CA2616109666
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822588-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822588C>G , CM000673.2:g.116822588C>G GRCh38
NC_000011.9:g.116693304C>G , CM000673.1:g.116693304C>G GRCh37
NC_000011.8:g.116198514C>G NCBI36
NG_012044.1:g.5708G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+71G>C MANE Select ENSP00000350425.3:n.176+71G>C
ENST00000357780.4:c.176+71G>C ENSP00000350425.3:n.176+71G>C
NM_000482.3:c.176+71G>C NP_000473.2:n.176+71G>C
NM_000482.4:c.176+71G>C MANE Select NP_000473.2:n.176+71G>C
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