Canonical Allele Identifier: CA382709999
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830824T>G , CM000673.2:g.116830824T>G GRCh38
NC_000011.9:g.116701540T>G , CM000673.1:g.116701540T>G GRCh37
NC_000011.8:g.116206750T>G NCBI36
NG_008949.1:g.5917T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.107T>G MANE Select ENSP00000227667.2:p.Met36Arg
ENST00000227667.7:c.107T>G ENSP00000227667.2:p.Met36Arg
ENST00000375345.3:c.161T>G ENSP00000364494.1:p.Met54Arg
ENST00000433777.5:c.107T>G ENSP00000410614.1:p.Met36Arg
ENST00000470144.1:n.139T>G
ENST00000630701.1:c.161T>G ENSP00000486182.1:p.Met54Arg
NM_000040.1:c.107T>G NP_000031.1:p.Met36Arg
NM_000040.2:c.107T>G NP_000031.1:p.Met36Arg
NM_000040.3:c.107T>G MANE Select NP_000031.1:p.Met36Arg