Canonical Allele Identifier: CA477048360
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116701340C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830624C>T , CM000673.2:g.116830624C>T GRCh38
NC_000011.9:g.116701340C>T , CM000673.1:g.116701340C>T GRCh37
NC_000011.8:g.116206550C>T NCBI36
NG_008949.1:g.5717C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.42C>T MANE Select ENSP00000227667.2:p.Leu14=
ENST00000227667.7:c.42C>T ENSP00000227667.2:p.Leu14=
ENST00000375345.3:c.96C>T ENSP00000364494.1:p.Leu32=
ENST00000433777.5:c.42C>T ENSP00000410614.1:p.Leu14=
ENST00000470144.1:n.74C>T
ENST00000630701.1:c.96C>T ENSP00000486182.1:p.Leu32=
NM_000040.1:c.42C>T NP_000031.1:p.Leu14=
NM_000040.2:c.42C>T NP_000031.1:p.Leu14=
NM_000040.3:c.42C>T MANE Select NP_000031.1:p.Leu14=