Canonical Allele Identifier: CA414795989
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692848
ClinVar RCV Id: RCV000854178
dbSNP Id: rs878942289
MyVariant Identifiers: chrMT:g.8411A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8411A>G , J01415.2:m.8411A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.46A>G ENSP00000355265.1:p.Ile16Val
Search 100 bp 5'
Search 100 bp 3'