Canonical Allele Identifier: CA382711236
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703518A>C (hg19) chr11:g.116832802A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832802A>C , CM000673.2:g.116832802A>C GRCh38
NC_000011.9:g.116703518A>C , CM000673.1:g.116703518A>C GRCh37
NC_000011.8:g.116208728A>C NCBI36
NG_008949.1:g.7895A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.218A>C MANE Select ENSP00000227667.2:p.Tyr73Ser
ENST00000227667.7:c.218A>C ENSP00000227667.2:p.Tyr73Ser
ENST00000375345.3:c.272A>C ENSP00000364494.1:p.Tyr91Ser
ENST00000630701.1:c.272A>C ENSP00000486182.1:p.Tyr91Ser
NM_000040.1:c.218A>C NP_000031.1:p.Tyr73Ser
NM_000040.2:c.218A>C NP_000031.1:p.Tyr73Ser
NM_000040.3:c.218A>C MANE Select NP_000031.1:p.Tyr73Ser
Search 100 bp 5'
Search 100 bp 3'