Canonical Allele Identifier: CA2002760253
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs754046943

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832729A>C , CM000673.2:g.116832729A>C GRCh38
NC_000011.9:g.116703445A>C , CM000673.1:g.116703445A>C GRCh37
NC_000011.8:g.116208655A>C NCBI36
NG_008949.1:g.7822A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.180-35A>C MANE Select ENSP00000227667.2:n.180-35A>C
ENST00000227667.7:c.180-35A>C ENSP00000227667.2:n.180-35A>C
ENST00000375345.3:c.234-35A>C ENSP00000364494.1:n.234-35A>C
ENST00000630701.1:c.234-35A>C ENSP00000486182.1:n.234-35A>C
NM_000040.1:c.180-35A>C NP_000031.1:n.180-35A>C
NM_000040.2:c.180-35A>C NP_000031.1:n.180-35A>C
NM_000040.3:c.180-35A>C MANE Select NP_000031.1:n.180-35A>C