Canonical Allele Identifier: CA229306566
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs765355262
gnomAD v4: 11-116822741-A-G
MyVariant Identifiers: chr11:g.116693457A>G (hg19) chr11:g.116822741A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822741A>G , CM000673.2:g.116822741A>G GRCh38
NC_000011.9:g.116693457A>G , CM000673.1:g.116693457A>G GRCh37
NC_000011.8:g.116198667A>G NCBI36
NG_012044.1:g.5555T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.94T>C MANE Select ENSP00000350425.3:p.Trp32Arg
ENST00000357780.4:c.94T>C ENSP00000350425.3:p.Trp32Arg
NM_000482.3:c.94T>C NP_000473.2:p.Trp32Arg
NM_000482.4:c.94T>C MANE Select NP_000473.2:p.Trp32Arg
Search 100 bp 5'
Search 100 bp 3'