Canonical Allele Identifier: CA2616110948
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830742T>G , CM000673.2:g.116830742T>G GRCh38
NC_000011.9:g.116701458T>G , CM000673.1:g.116701458T>G GRCh37
NC_000011.8:g.116206668T>G NCBI36
NG_008949.1:g.5835T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.56-31T>G MANE Select ENSP00000227667.2:n.56-31T>G
ENST00000227667.7:c.56-31T>G ENSP00000227667.2:n.56-31T>G
ENST00000375345.3:c.110-31T>G ENSP00000364494.1:n.110-31T>G
ENST00000433777.5:c.56-31T>G ENSP00000410614.1:n.56-31T>G
ENST00000470144.1:n.88-31T>G
ENST00000630701.1:c.110-31T>G ENSP00000486182.1:n.110-31T>G
NM_000040.1:c.56-31T>G NP_000031.1:n.56-31T>G
NM_000040.2:c.56-31T>G NP_000031.1:n.56-31T>G
NM_000040.3:c.56-31T>G MANE Select NP_000031.1:n.56-31T>G