Canonical Allele Identifier: CA382711648

Gene: APOC3

Linked Data

• dbSNP Id: rs1941477792
• gnomAD v4: 11-116832861-C-T
• MyVariant Identifiers: chr11:g.116703577C>T (hg19) ; chr11:g.116832861C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832861C>T , CM000673.2:g.116832861C>T	GRCh38
NC_000011.9:g.116703577C>T , CM000673.1:g.116703577C>T	GRCh37
NC_000011.8:g.116208787C>T	NCBI36
NG_008949.1:g.7954C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.277C>T MANE Select	ENSP00000227667.2:p.Pro93Ser
ENST00000227667.7:c.277C>T	ENSP00000227667.2:p.Pro93Ser
ENST00000375345.3:c.331C>T	ENSP00000364494.1:p.Pro111Ser
ENST00000630701.1:c.331C>T	ENSP00000486182.1:p.Pro111Ser
NM_000040.1:c.277C>T	NP_000031.1:p.Pro93Ser
NM_000040.2:c.277C>T	NP_000031.1:p.Pro93Ser
NM_000040.3:c.277C>T MANE Select	NP_000031.1:p.Pro93Ser