Canonical Allele Identifier: CA601826043
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1267319833

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833000T>C , CM000673.2:g.116833000T>C GRCh38
NC_000011.9:g.116703716T>C , CM000673.1:g.116703716T>C GRCh37
NC_000011.8:g.116208926T>C NCBI36
NG_008949.1:g.8093T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*116T>C MANE Select ENSP00000227667.2:n.*116T>C
ENST00000227667.7:c.*116T>C ENSP00000227667.2:n.*116T>C
ENST00000375345.3:c.*116T>C ENSP00000364494.1:n.*116T>C
ENST00000630701.1:c.470T>C ENSP00000486182.1:n.470T>C
NM_000040.1:c.*116T>C NP_000031.1:n.*116T>C
NM_000040.2:c.*116T>C NP_000031.1:n.*116T>C
NM_000040.3:c.*116T>C MANE Select NP_000031.1:n.*116T>C