Canonical Allele Identifier: CA414801848
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693053
ClinVar RCV Id: RCV000854397
dbSNP Id: rs1556423589
MyVariant Identifiers: chrMT:g.9010G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9010G>A , J01415.2:m.9010G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.484G>A ENSP00000354632.2:p.Ala162Thr