Canonical Allele Identifier: CA2616110911

Gene: APOC3

Linked Data

• gnomAD v4: 11-116830651-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830651G>T , CM000673.2:g.116830651G>T	GRCh38
NC_000011.9:g.116701367G>T , CM000673.1:g.116701367G>T	GRCh37
NC_000011.8:g.116206577G>T	NCBI36
NG_008949.1:g.5744G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.55+14G>T MANE Select	ENSP00000227667.2:n.55+14G>T
ENST00000227667.7:c.55+14G>T	ENSP00000227667.2:n.55+14G>T
ENST00000375345.3:c.109+14G>T	ENSP00000364494.1:n.109+14G>T
ENST00000433777.5:c.55+14G>T	ENSP00000410614.1:n.55+14G>T
ENST00000470144.1:n.87+14G>T
ENST00000630701.1:c.109+14G>T	ENSP00000486182.1:n.109+14G>T
NM_000040.1:c.55+14G>T	NP_000031.1:n.55+14G>T
NM_000040.2:c.55+14G>T	NP_000031.1:n.55+14G>T
NM_000040.3:c.55+14G>T MANE Select	NP_000031.1:n.55+14G>T