Canonical Allele Identifier: CA2002760398
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941479964
gnomAD v4: 11-116833013-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833013G>T , CM000673.2:g.116833013G>T GRCh38
NC_000011.9:g.116703729G>T , CM000673.1:g.116703729G>T GRCh37
NC_000011.8:g.116208939G>T NCBI36
NG_008949.1:g.8106G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*129G>T MANE Select ENSP00000227667.2:n.*129G>T
ENST00000227667.7:c.*129G>T ENSP00000227667.2:n.*129G>T
ENST00000375345.3:c.*129G>T ENSP00000364494.1:n.*129G>T
ENST00000630701.1:c.483G>T ENSP00000486182.1:n.483G>T
NM_000040.1:c.*129G>T NP_000031.1:n.*129G>T
NM_000040.2:c.*129G>T NP_000031.1:n.*129G>T
NM_000040.3:c.*129G>T MANE Select NP_000031.1:n.*129G>T
Search 100 bp 5'
Search 100 bp 3'