Canonical Allele Identifier: CA2002758820
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941435767
gnomAD v4: 11-116830649-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830649G>C , CM000673.2:g.116830649G>C GRCh38
NC_000011.9:g.116701365G>C , CM000673.1:g.116701365G>C GRCh37
NC_000011.8:g.116206575G>C NCBI36
NG_008949.1:g.5742G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.55+12G>C MANE Select ENSP00000227667.2:n.55+12G>C
ENST00000227667.7:c.55+12G>C ENSP00000227667.2:n.55+12G>C
ENST00000375345.3:c.109+12G>C ENSP00000364494.1:n.109+12G>C
ENST00000433777.5:c.55+12G>C ENSP00000410614.1:n.55+12G>C
ENST00000470144.1:n.87+12G>C
ENST00000630701.1:c.109+12G>C ENSP00000486182.1:n.109+12G>C
NM_000040.1:c.55+12G>C NP_000031.1:n.55+12G>C
NM_000040.2:c.55+12G>C NP_000031.1:n.55+12G>C
NM_000040.3:c.55+12G>C MANE Select NP_000031.1:n.55+12G>C
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