Canonical Allele Identifier: CA2616111303

Gene: APOC3

Linked Data

• gnomAD v4: 11-116832909-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832909G>T , CM000673.2:g.116832909G>T	GRCh38
NC_000011.9:g.116703625G>T , CM000673.1:g.116703625G>T	GRCh37
NC_000011.8:g.116208835G>T	NCBI36
NG_008949.1:g.8002G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.*25G>T MANE Select	ENSP00000227667.2:n.*25G>T
ENST00000227667.7:c.*25G>T	ENSP00000227667.2:n.*25G>T
ENST00000375345.3:c.*25G>T	ENSP00000364494.1:n.*25G>T
ENST00000630701.1:c.379G>T	ENSP00000486182.1:n.379G>T
NM_000040.1:c.*25G>T	NP_000031.1:n.*25G>T
NM_000040.2:c.*25G>T	NP_000031.1:n.*25G>T
NM_000040.3:c.*25G>T MANE Select	NP_000031.1:n.*25G>T