Canonical Allele Identifier: CA382711550
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703560T>G (hg19) chr11:g.116832844T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832844T>G , CM000673.2:g.116832844T>G GRCh38
NC_000011.9:g.116703560T>G , CM000673.1:g.116703560T>G GRCh37
NC_000011.8:g.116208770T>G NCBI36
NG_008949.1:g.7937T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.260T>G MANE Select ENSP00000227667.2:p.Leu87Trp
ENST00000227667.7:c.260T>G ENSP00000227667.2:p.Leu87Trp
ENST00000375345.3:c.314T>G ENSP00000364494.1:p.Leu105Trp
ENST00000630701.1:c.314T>G ENSP00000486182.1:p.Leu105Trp
NM_000040.1:c.260T>G NP_000031.1:p.Leu87Trp
NM_000040.2:c.260T>G NP_000031.1:p.Leu87Trp
NM_000040.3:c.260T>G MANE Select NP_000031.1:p.Leu87Trp
Search 100 bp 5'
Search 100 bp 3'