Canonical Allele Identifier: CA2002758816
Gene: APOC3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830645C= , CM000673.2:g.116830645C= GRCh38
NC_000011.9:g.116701361C= , CM000673.1:g.116701361C= GRCh37
NC_000011.8:g.116206571C= NCBI36
NG_008949.1:g.5738C=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.55+8C= MANE Select ENSP00000227667.2:n.55+8C=
ENST00000227667.7:c.55+8C= ENSP00000227667.2:n.55+8C=
ENST00000375345.3:c.109+8C= ENSP00000364494.1:n.109+8C=
ENST00000433777.5:c.55+8C= ENSP00000410614.1:n.55+8C=
ENST00000470144.1:n.87+8C=
ENST00000630701.1:c.109+8C= ENSP00000486182.1:n.109+8C=
NM_000040.1:c.55+8C= NP_000031.1:n.55+8C=
NM_000040.2:c.55+8C= NP_000031.1:n.55+8C=
NM_000040.3:c.55+8C= MANE Select NP_000031.1:n.55+8C=
Search 100 bp 5'
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