Canonical Allele Identifier: CA6289676
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs754046943

Genomic Alleles

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

Transcript Alleles

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