Canonical Allele Identifier: CA382711207
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832796A>C , CM000673.2:g.116832796A>C GRCh38
NC_000011.9:g.116703512A>C , CM000673.1:g.116703512A>C GRCh37
NC_000011.8:g.116208722A>C NCBI36
NG_008949.1:g.7889A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.212A>C MANE Select ENSP00000227667.2:p.Lys71Thr
ENST00000227667.7:c.212A>C ENSP00000227667.2:p.Lys71Thr
ENST00000375345.3:c.266A>C ENSP00000364494.1:p.Lys89Thr
ENST00000630701.1:c.266A>C ENSP00000486182.1:p.Lys89Thr
NM_000040.1:c.212A>C NP_000031.1:p.Lys71Thr
NM_000040.2:c.212A>C NP_000031.1:p.Lys71Thr
NM_000040.3:c.212A>C MANE Select NP_000031.1:p.Lys71Thr