Canonical Allele Identifier: CA382711548
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941477541

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.260T>C MANE Select ENSP00000227667.2:p.Leu87Ser
ENST00000227667.7:c.260T>C ENSP00000227667.2:p.Leu87Ser
ENST00000375345.3:c.314T>C ENSP00000364494.1:p.Leu105Ser
ENST00000630701.1:c.314T>C ENSP00000486182.1:p.Leu105Ser
NM_000040.1:c.260T>C NP_000031.1:p.Leu87Ser
NM_000040.2:c.260T>C NP_000031.1:p.Leu87Ser
NM_000040.3:c.260T>C MANE Select NP_000031.1:p.Leu87Ser