Canonical Allele Identifier: CA382709986
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830822C>G , CM000673.2:g.116830822C>G GRCh38
NC_000011.9:g.116701538C>G , CM000673.1:g.116701538C>G GRCh37
NC_000011.8:g.116206748C>G NCBI36
NG_008949.1:g.5915C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.105C>G MANE Select ENSP00000227667.2:p.Tyr35Ter
ENST00000227667.7:c.105C>G ENSP00000227667.2:p.Tyr35Ter
ENST00000375345.3:c.159C>G ENSP00000364494.1:p.Tyr53Ter
ENST00000433777.5:c.105C>G ENSP00000410614.1:p.Tyr35Ter
ENST00000470144.1:n.137C>G
ENST00000630701.1:c.159C>G ENSP00000486182.1:p.Tyr53Ter
NM_000040.1:c.105C>G NP_000031.1:p.Tyr35Ter
NM_000040.2:c.105C>G NP_000031.1:p.Tyr35Ter
NM_000040.3:c.105C>G MANE Select NP_000031.1:p.Tyr35Ter