Canonical Allele Identifier: CA2616110910
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116830646-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830646T>C , CM000673.2:g.116830646T>C GRCh38
NC_000011.9:g.116701362T>C , CM000673.1:g.116701362T>C GRCh37
NC_000011.8:g.116206572T>C NCBI36
NG_008949.1:g.5739T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.55+9T>C MANE Select ENSP00000227667.2:n.55+9T>C
ENST00000227667.7:c.55+9T>C ENSP00000227667.2:n.55+9T>C
ENST00000375345.3:c.109+9T>C ENSP00000364494.1:n.109+9T>C
ENST00000433777.5:c.55+9T>C ENSP00000410614.1:n.55+9T>C
ENST00000470144.1:n.87+9T>C
ENST00000630701.1:c.109+9T>C ENSP00000486182.1:n.109+9T>C
NM_000040.1:c.55+9T>C NP_000031.1:n.55+9T>C
NM_000040.2:c.55+9T>C NP_000031.1:n.55+9T>C
NM_000040.3:c.55+9T>C MANE Select NP_000031.1:n.55+9T>C
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