Canonical Allele Identifier: CA476868561
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693500T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822784T>C , CM000673.2:g.116822784T>C GRCh38
NC_000011.9:g.116693500T>C , CM000673.1:g.116693500T>C GRCh37
NC_000011.8:g.116198710T>C NCBI36
NG_012044.1:g.5512A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.51A>G MANE Select ENSP00000350425.3:p.Gly17=
ENST00000357780.4:c.51A>G ENSP00000350425.3:p.Gly17=
NM_000482.3:c.51A>G NP_000473.2:p.Gly17=
NM_000482.4:c.51A>G MANE Select NP_000473.2:p.Gly17=
Search 100 bp 5'
Search 100 bp 3'