Canonical Allele Identifier: CA2002760265
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941476094

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832754A>G , CM000673.2:g.116832754A>G GRCh38
NC_000011.9:g.116703470A>G , CM000673.1:g.116703470A>G GRCh37
NC_000011.8:g.116208680A>G NCBI36
NG_008949.1:g.7847A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.180-10A>G MANE Select ENSP00000227667.2:n.180-10A>G
ENST00000227667.7:c.180-10A>G ENSP00000227667.2:n.180-10A>G
ENST00000375345.3:c.234-10A>G ENSP00000364494.1:n.234-10A>G
ENST00000630701.1:c.234-10A>G ENSP00000486182.1:n.234-10A>G
NM_000040.1:c.180-10A>G NP_000031.1:n.180-10A>G
NM_000040.2:c.180-10A>G NP_000031.1:n.180-10A>G
NM_000040.3:c.180-10A>G MANE Select NP_000031.1:n.180-10A>G