Canonical Allele Identifier: CA601823648
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs1340165282
gnomAD v2: 11-116693299-A-G
gnomAD v3: 11-116822583-A-G
gnomAD v4: 11-116822583-A-G
MyVariant Identifiers: chr11:g.116693299A>G (hg19) chr11:g.116822583A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822583A>G , CM000673.2:g.116822583A>G GRCh38
NC_000011.9:g.116693299A>G , CM000673.1:g.116693299A>G GRCh37
NC_000011.8:g.116198509A>G NCBI36
NG_012044.1:g.5713T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.176+76T>C MANE Select ENSP00000350425.3:n.176+76T>C
ENST00000357780.4:c.176+76T>C ENSP00000350425.3:n.176+76T>C
NM_000482.3:c.176+76T>C NP_000473.2:n.176+76T>C
NM_000482.4:c.176+76T>C MANE Select NP_000473.2:n.176+76T>C
Search 100 bp 5'
Search 100 bp 3'