Canonical Allele Identifier: CA672179999
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs1024506294
MyVariant Identifiers: chr11:g.116693272T>C (hg19) chr11:g.116822556T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822556T>C , CM000673.2:g.116822556T>C GRCh38
NC_000011.9:g.116693272T>C , CM000673.1:g.116693272T>C GRCh37
NC_000011.8:g.116198482T>C NCBI36
NG_012044.1:g.5740A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+103A>G MANE Select ENSP00000350425.3:n.176+103A>G
ENST00000357780.4:c.176+103A>G ENSP00000350425.3:n.176+103A>G
NM_000482.3:c.176+103A>G NP_000473.2:n.176+103A>G
NM_000482.4:c.176+103A>G MANE Select NP_000473.2:n.176+103A>G
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