Canonical Allele Identifier: CA2616110917
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116830661-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830661T>G , CM000673.2:g.116830661T>G GRCh38
NC_000011.9:g.116701377T>G , CM000673.1:g.116701377T>G GRCh37
NC_000011.8:g.116206587T>G NCBI36
NG_008949.1:g.5754T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.55+24T>G MANE Select ENSP00000227667.2:n.55+24T>G
ENST00000227667.7:c.55+24T>G ENSP00000227667.2:n.55+24T>G
ENST00000375345.3:c.109+24T>G ENSP00000364494.1:n.109+24T>G
ENST00000433777.5:c.55+24T>G ENSP00000410614.1:n.55+24T>G
ENST00000470144.1:n.87+24T>G
ENST00000630701.1:c.109+24T>G ENSP00000486182.1:n.109+24T>G
NM_000040.1:c.55+24T>G NP_000031.1:n.55+24T>G
NM_000040.2:c.55+24T>G NP_000031.1:n.55+24T>G
NM_000040.3:c.55+24T>G MANE Select NP_000031.1:n.55+24T>G
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