Canonical Allele Identifier: CA16603225
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 376981
ClinVar RCV Id: RCV000427129
dbSNP Id: rs1057520102
MyVariant Identifiers: chrMT:g.8816A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8816A>G , J01415.2:m.8816A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.290A>G ENSP00000354632.2:p.Gln97Arg