Canonical Allele Identifier: CA2002760364
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941479366
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832960T>C , CM000673.2:g.116832960T>C GRCh38
NC_000011.9:g.116703676T>C , CM000673.1:g.116703676T>C GRCh37
NC_000011.8:g.116208886T>C NCBI36
NG_008949.1:g.8053T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*76T>C MANE Select ENSP00000227667.2:n.*76T>C
ENST00000227667.7:c.*76T>C ENSP00000227667.2:n.*76T>C
ENST00000375345.3:c.*76T>C ENSP00000364494.1:n.*76T>C
ENST00000630701.1:c.430T>C ENSP00000486182.1:n.430T>C
NM_000040.1:c.*76T>C NP_000031.1:n.*76T>C
NM_000040.2:c.*76T>C NP_000031.1:n.*76T>C
NM_000040.3:c.*76T>C MANE Select NP_000031.1:n.*76T>C
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