Canonical Allele Identifier: CA2558628937

Gene: APOC3

Linked Data

• gnomAD v4: 11-116832965-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832965G>T , CM000673.2:g.116832965G>T	GRCh38
NC_000011.9:g.116703681G>T , CM000673.1:g.116703681G>T	GRCh37
NC_000011.8:g.116208891G>T	NCBI36
NG_008949.1:g.8058G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.*81G>T MANE Select	ENSP00000227667.2:n.*81G>T
ENST00000227667.7:c.*81G>T	ENSP00000227667.2:n.*81G>T
ENST00000375345.3:c.*81G>T	ENSP00000364494.1:n.*81G>T
ENST00000630701.1:c.435G>T	ENSP00000486182.1:n.435G>T
NM_000040.1:c.*81G>T	NP_000031.1:n.*81G>T
NM_000040.2:c.*81G>T	NP_000031.1:n.*81G>T
NM_000040.3:c.*81G>T MANE Select	NP_000031.1:n.*81G>T