Canonical Allele Identifier: CA414801926
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693059
ClinVar RCV Id: RCV000854403
dbSNP Id: rs1603221990
MyVariant Identifiers: chrMT:g.9028C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9028C>T , J01415.2:m.9028C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.502C>T ENSP00000354632.2:p.His168Tyr
Search 100 bp 5'
Search 100 bp 3'