Canonical Allele Identifier: CA382705084
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs1181491256
gnomAD v2: 11-116693468-G-C
gnomAD v3: 11-116822752-G-C
gnomAD v4: 11-116822752-G-C
MyVariant Identifiers: chr11:g.116693468G>C (hg19) chr11:g.116822752G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822752G>C , CM000673.2:g.116822752G>C GRCh38
NC_000011.9:g.116693468G>C , CM000673.1:g.116693468G>C GRCh37
NC_000011.8:g.116198678G>C NCBI36
NG_012044.1:g.5544C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.83C>G MANE Select ENSP00000350425.3:p.Ala28Gly
ENST00000357780.4:c.83C>G ENSP00000350425.3:p.Ala28Gly
NM_000482.3:c.83C>G NP_000473.2:p.Ala28Gly
NM_000482.4:c.83C>G MANE Select NP_000473.2:p.Ala28Gly
Search 100 bp 5'
Search 100 bp 3'