Canonical Allele Identifier: CA414799093
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693032
ClinVar RCV Id: RCV000854373
dbSNP Id: rs1603221929
MyVariant Identifiers: chrMT:g.8944A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8944A>G , J01415.2:m.8944A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361899.2:c.418A>G ENSP00000354632.2:p.Ile140Val
Search 100 bp 5'
Search 100 bp 3'