Canonical Allele Identifier: CA382711096
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703486G>C (hg19) chr11:g.116832770G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832770G>C , CM000673.2:g.116832770G>C GRCh38
NC_000011.9:g.116703486G>C , CM000673.1:g.116703486G>C GRCh37
NC_000011.8:g.116208696G>C NCBI36
NG_008949.1:g.7863G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.186G>C MANE Select ENSP00000227667.2:p.Trp62Cys
ENST00000227667.7:c.186G>C ENSP00000227667.2:p.Trp62Cys
ENST00000375345.3:c.240G>C ENSP00000364494.1:p.Trp80Cys
ENST00000630701.1:c.240G>C ENSP00000486182.1:p.Trp80Cys
NM_000040.1:c.186G>C NP_000031.1:p.Trp62Cys
NM_000040.2:c.186G>C NP_000031.1:p.Trp62Cys
NM_000040.3:c.186G>C MANE Select NP_000031.1:p.Trp62Cys
Search 100 bp 5'
Search 100 bp 3'