Canonical Allele Identifier: CA414801836
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693052
ClinVar RCV Id: RCV000854396
dbSNP Id: rs1603221973
MyVariant Identifiers: chrMT:g.9007A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9007A>T , J01415.2:m.9007A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.481A>T ENSP00000354632.2:p.Thr161Ser
Search 100 bp 5'
Search 100 bp 3'