Canonical Allele Identifier: CA382706603
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693498G>A (hg19) chr11:g.116822782G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822782G>A , CM000673.2:g.116822782G>A GRCh38
NC_000011.9:g.116693498G>A , CM000673.1:g.116693498G>A GRCh37
NC_000011.8:g.116198708G>A NCBI36
NG_012044.1:g.5514C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.53C>T MANE Select ENSP00000350425.3:p.Ala18Val
ENST00000357780.4:c.53C>T ENSP00000350425.3:p.Ala18Val
NM_000482.3:c.53C>T NP_000473.2:p.Ala18Val
NM_000482.4:c.53C>T MANE Select NP_000473.2:p.Ala18Val
Search 100 bp 5'
Search 100 bp 3'