Canonical Allele Identifier: CA477048354
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116701334G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830618G>T , CM000673.2:g.116830618G>T GRCh38
NC_000011.9:g.116701334G>T , CM000673.1:g.116701334G>T GRCh37
NC_000011.8:g.116206544G>T NCBI36
NG_008949.1:g.5711G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.36G>T MANE Select ENSP00000227667.2:p.Leu12=
ENST00000227667.7:c.36G>T ENSP00000227667.2:p.Leu12=
ENST00000375345.3:c.90G>T ENSP00000364494.1:p.Leu30=
ENST00000433777.5:c.36G>T ENSP00000410614.1:p.Leu12=
ENST00000470144.1:n.68G>T
ENST00000630701.1:c.90G>T ENSP00000486182.1:p.Leu30=
NM_000040.1:c.36G>T NP_000031.1:p.Leu12=
NM_000040.2:c.36G>T NP_000031.1:p.Leu12=
NM_000040.3:c.36G>T MANE Select NP_000031.1:p.Leu12=