Canonical Allele Identifier: CA382711790
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703592G>T (hg19) chr11:g.116832876G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832876G>T , CM000673.2:g.116832876G>T GRCh38
NC_000011.9:g.116703592G>T , CM000673.1:g.116703592G>T GRCh37
NC_000011.8:g.116208802G>T NCBI36
NG_008949.1:g.7969G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.292G>T MANE Select ENSP00000227667.2:p.Ala98Ser
ENST00000227667.7:c.292G>T ENSP00000227667.2:p.Ala98Ser
ENST00000375345.3:c.346G>T ENSP00000364494.1:p.Ala116Ser
ENST00000630701.1:c.346G>T ENSP00000486182.1:p.Ala116Ser
NM_000040.1:c.292G>T NP_000031.1:p.Ala98Ser
NM_000040.2:c.292G>T NP_000031.1:p.Ala98Ser
NM_000040.3:c.292G>T MANE Select NP_000031.1:p.Ala98Ser
Search 100 bp 5'
Search 100 bp 3'