Canonical Allele Identifier: CA414802396
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693121
ClinVar RCV Id: RCV000854472
dbSNP Id: rs1603222162
MyVariant Identifiers: chrMT:g.9194A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9194A>G , J01415.2:m.9194A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.668A>G ENSP00000354632.2:p.His223Arg
Search 100 bp 5'
Search 100 bp 3'