Canonical Allele Identifier: CA6289696
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs774709008

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832839G>C , CM000673.2:g.116832839G>C GRCh38
NC_000011.9:g.116703555G>C , CM000673.1:g.116703555G>C GRCh37
NC_000011.8:g.116208765G>C NCBI36
NG_008949.1:g.7932G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.255G>C MANE Select ENSP00000227667.2:p.Trp85Cys
ENST00000227667.7:c.255G>C ENSP00000227667.2:p.Trp85Cys
ENST00000375345.3:c.309G>C ENSP00000364494.1:p.Trp103Cys
ENST00000630701.1:c.309G>C ENSP00000486182.1:p.Trp103Cys
NM_000040.1:c.255G>C NP_000031.1:p.Trp85Cys
NM_000040.2:c.255G>C NP_000031.1:p.Trp85Cys
NM_000040.3:c.255G>C MANE Select NP_000031.1:p.Trp85Cys