Canonical Allele Identifier: CA601825990

Gene: APOC3

Linked Data

• dbSNP Id: rs1232736617
• gnomAD v2: 11-116703467-C-T
• gnomAD v4: 11-116832751-C-T
• MyVariant Identifiers: chr11:g.116703467C>T (hg19) ; chr11:g.116832751C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832751C>T , CM000673.2:g.116832751C>T	GRCh38
NC_000011.9:g.116703467C>T , CM000673.1:g.116703467C>T	GRCh37
NC_000011.8:g.116208677C>T	NCBI36
NG_008949.1:g.7844C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.180-13C>T MANE Select	ENSP00000227667.2:n.180-13C>T
ENST00000227667.7:c.180-13C>T	ENSP00000227667.2:n.180-13C>T
ENST00000375345.3:c.234-13C>T	ENSP00000364494.1:n.234-13C>T
ENST00000630701.1:c.234-13C>T	ENSP00000486182.1:n.234-13C>T
NM_000040.1:c.180-13C>T	NP_000031.1:n.180-13C>T
NM_000040.2:c.180-13C>T	NP_000031.1:n.180-13C>T
NM_000040.3:c.180-13C>T MANE Select	NP_000031.1:n.180-13C>T