Canonical Allele Identifier: CA337097903
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692878
ClinVar RCV Id: RCV000854208
dbSNP Id: rs879247004
MyVariant Identifiers: chrMT:g.8502A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8502A>G , J01415.2:m.8502A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.137A>G ENSP00000355265.1:p.Asn46Ser
Search 100 bp 5'
Search 100 bp 3'