Canonical Allele Identifier: CA414797121
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692937
ClinVar RCV Id: RCV000854273
dbSNP Id: rs1603221662
MyVariant Identifiers: chrMT:g.8641A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8641A>G , J01415.2:m.8641A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.115A>G ENSP00000354632.2:p.Asn39Asp