Canonical Allele Identifier: CA382711810
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832879G>A , CM000673.2:g.116832879G>A GRCh38
NC_000011.9:g.116703595G>A , CM000673.1:g.116703595G>A GRCh37
NC_000011.8:g.116208805G>A NCBI36
NG_008949.1:g.7972G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.295G>A MANE Select ENSP00000227667.2:p.Ala99Thr
ENST00000227667.7:c.295G>A ENSP00000227667.2:p.Ala99Thr
ENST00000375345.3:c.349G>A ENSP00000364494.1:p.Ala117Thr
ENST00000630701.1:c.349G>A ENSP00000486182.1:p.Ala117Thr
NM_000040.1:c.295G>A NP_000031.1:p.Ala99Thr
NM_000040.2:c.295G>A NP_000031.1:p.Ala99Thr
NM_000040.3:c.295G>A MANE Select NP_000031.1:p.Ala99Thr