Canonical Allele Identifier: CA414795927
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692843
ClinVar RCV Id: RCV000854173
dbSNP Id: rs1603221456
MyVariant Identifiers: chrMT:g.8397C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8397C>G , J01415.2:m.8397C>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.32C>G ENSP00000355265.1:p.Thr11Ser
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