Canonical Allele Identifier: CA6289706

Gene: APOC3

Linked Data

• dbSNP Id: rs144573427
• ExAC: 11:116703588 C / T
• gnomAD v2: 11-116703588-C-T
• gnomAD v3: 11-116832872-C-T
• gnomAD v4: 11-116832872-C-T
• MyVariant Identifiers: chr11:g.116703588C>T (hg19) ; chr11:g.116832872C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832872C>T , CM000673.2:g.116832872C>T	GRCh38
NC_000011.9:g.116703588C>T , CM000673.1:g.116703588C>T	GRCh37
NC_000011.8:g.116208798C>T	NCBI36
NG_008949.1:g.7965C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.288C>T MANE Select	ENSP00000227667.2:p.Ala96=
ENST00000227667.7:c.288C>T	ENSP00000227667.2:p.Ala96=
ENST00000375345.3:c.342C>T	ENSP00000364494.1:p.Ala114=
ENST00000630701.1:c.342C>T	ENSP00000486182.1:p.Ala114=
NM_000040.1:c.288C>T	NP_000031.1:p.Ala96=
NM_000040.2:c.288C>T	NP_000031.1:p.Ala96=
NM_000040.3:c.288C>T MANE Select	NP_000031.1:p.Ala96=