Canonical Allele Identifier: CA382711677
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703581C>A (hg19) chr11:g.116832865C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832865C>A , CM000673.2:g.116832865C>A GRCh38
NC_000011.9:g.116703581C>A , CM000673.1:g.116703581C>A GRCh37
NC_000011.8:g.116208791C>A NCBI36
NG_008949.1:g.7958C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.281C>A MANE Select ENSP00000227667.2:p.Thr94Asn
ENST00000227667.7:c.281C>A ENSP00000227667.2:p.Thr94Asn
ENST00000375345.3:c.335C>A ENSP00000364494.1:p.Thr112Asn
ENST00000630701.1:c.335C>A ENSP00000486182.1:p.Thr112Asn
NM_000040.1:c.281C>A NP_000031.1:p.Thr94Asn
NM_000040.2:c.281C>A NP_000031.1:p.Thr94Asn
NM_000040.3:c.281C>A MANE Select NP_000031.1:p.Thr94Asn
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