Canonical Allele Identifier: CA672180005
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs13306177
gnomAD v4: 11-116822564-G-C
MyVariant Identifiers: chr11:g.116693280G>C (hg19) chr11:g.116822564G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822564G>C , CM000673.2:g.116822564G>C GRCh38
NC_000011.9:g.116693280G>C , CM000673.1:g.116693280G>C GRCh37
NC_000011.8:g.116198490G>C NCBI36
NG_012044.1:g.5732C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.176+95C>G MANE Select ENSP00000350425.3:n.176+95C>G
ENST00000357780.4:c.176+95C>G ENSP00000350425.3:n.176+95C>G
NM_000482.3:c.176+95C>G NP_000473.2:n.176+95C>G
NM_000482.4:c.176+95C>G MANE Select NP_000473.2:n.176+95C>G
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