Canonical Allele Identifier: CA476868920
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703489G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832773G>A , CM000673.2:g.116832773G>A GRCh38
NC_000011.9:g.116703489G>A , CM000673.1:g.116703489G>A GRCh37
NC_000011.8:g.116208699G>A NCBI36
NG_008949.1:g.7866G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.189G>A MANE Select ENSP00000227667.2:p.Val63=
ENST00000227667.7:c.189G>A ENSP00000227667.2:p.Val63=
ENST00000375345.3:c.243G>A ENSP00000364494.1:p.Val81=
ENST00000630701.1:c.243G>A ENSP00000486182.1:p.Val81=
NM_000040.1:c.189G>A NP_000031.1:p.Val63=
NM_000040.2:c.189G>A NP_000031.1:p.Val63=
NM_000040.3:c.189G>A MANE Select NP_000031.1:p.Val63=