Canonical Allele Identifier: CA414798049
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692982
ClinVar RCV Id: RCV000854321
dbSNP Id: rs1603221801
MyVariant Identifiers: chrMT:g.8782G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8782G>A , J01415.2:m.8782G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.256G>A ENSP00000354632.2:p.Gly86Arg