Canonical Allele Identifier: CA382704565
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693374C>T (hg19) chr11:g.116822658C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822658C>T , CM000673.2:g.116822658C>T GRCh38
NC_000011.9:g.116693374C>T , CM000673.1:g.116693374C>T GRCh37
NC_000011.8:g.116198584C>T NCBI36
NG_012044.1:g.5638G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+1G>A MANE Select ENSP00000350425.3:n.176+1G>A
ENST00000357780.4:c.176+1G>A ENSP00000350425.3:n.176+1G>A
NM_000482.3:c.176+1G>A NP_000473.2:n.176+1G>A
NM_000482.4:c.176+1G>A MANE Select NP_000473.2:n.176+1G>A
Search 100 bp 5'
Search 100 bp 3'