Canonical Allele Identifier: CA414797282
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692946
ClinVar RCV Id: RCV000854283
dbSNP Id: rs1603221681
MyVariant Identifiers: chrMT:g.8666A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8666A>G , J01415.2:m.8666A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.140A>G ENSP00000354632.2:p.Gln47Arg
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