Canonical Allele Identifier: CA414803873
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693243
ClinVar RCV Id: RCV000854598
dbSNP Id: rs1603222555
MyVariant Identifiers: chrMT:g.9862T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9862T>A , J01415.2:m.9862T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.656T>A ENSP00000354982.2:p.Phe219Tyr
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