Canonical Allele Identifier: CA414796088
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692857
ClinVar RCV Id: RCV000854187
dbSNP Id: rs1603221481
MyVariant Identifiers: chrMT:g.8435A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8435A>T , J01415.2:m.8435A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.70A>T ENSP00000355265.1:p.Thr24Ser
Search 100 bp 5'
Search 100 bp 3'