Canonical Allele Identifier: CA414795858
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692838
ClinVar RCV Id: RCV000854166
dbSNP Id: rs1603221438
MyVariant Identifiers: chrMT:g.8381A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8381A>T , J01415.2:m.8381A>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361851.1:c.16A>T ENSP00000355265.1:p.Thr6Ser
Search 100 bp 5'
Search 100 bp 3'