Canonical Allele Identifier: CA382709624
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830614T>C , CM000673.2:g.116830614T>C GRCh38
NC_000011.9:g.116701330T>C , CM000673.1:g.116701330T>C GRCh37
NC_000011.8:g.116206540T>C NCBI36
NG_008949.1:g.5707T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.32T>C MANE Select ENSP00000227667.2:p.Leu11Pro
ENST00000227667.7:c.32T>C ENSP00000227667.2:p.Leu11Pro
ENST00000375345.3:c.86T>C ENSP00000364494.1:p.Leu29Pro
ENST00000433777.5:c.32T>C ENSP00000410614.1:p.Leu11Pro
ENST00000470144.1:n.64T>C
ENST00000630701.1:c.86T>C ENSP00000486182.1:p.Leu29Pro
NM_000040.1:c.32T>C NP_000031.1:p.Leu11Pro
NM_000040.2:c.32T>C NP_000031.1:p.Leu11Pro
NM_000040.3:c.32T>C MANE Select NP_000031.1:p.Leu11Pro