Canonical Allele Identifier: CA476868921
Gene: APOC3 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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