Canonical Allele Identifier: CA6289069
Gene: APOA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2452816
ClinVar RCV Id: RCV003177590
dbSNP Id: rs771125152
ExAC: 11:116661450 G / T
gnomAD v2: 11-116661450-G-T
gnomAD v4: 11-116790734-G-T
MyVariant Identifiers: chr11:g.116661450G>T (hg19) chr11:g.116790734G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790734G>T , CM000673.2:g.116790734G>T GRCh38
NC_000011.9:g.116661450G>T , CM000673.1:g.116661450G>T GRCh37
NC_000011.8:g.116166660G>T NCBI36
NG_015894.1:g.6687C>A
NG_015894.2:g.6687C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.495C>A MANE Select ENSP00000227665.4:p.Gly165=
ENST00000433069.2:c.495C>A ENSP00000399701.2:p.Gly165=
ENST00000673688.1:c.579C>A ENSP00000501141.1:p.Gly193=
ENST00000227665.8:c.495C>A ENSP00000227665.4:p.Gly165=
ENST00000542499.5:c.495C>A ENSP00000445002.1:p.Gly165=
NM_001166598.1:c.495C>A NP_001160070.1:p.Gly165=
NM_052968.4:c.495C>A NP_443200.2:p.Gly165=
NM_001166598.2:c.495C>A NP_001160070.1:p.Gly165=
NM_001371904.1:c.495C>A MANE Select NP_001358833.1:p.Gly165=
NM_052968.5:c.495C>A NP_443200.2:p.Gly165=
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