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Canonical Allele Identifier:
CA414796712
Gene: MT-ATP8
HGNC
NCBI
MT-ATP6
HGNC
NCBI
Linked Data
ClinVar Variation Id:
692903
ClinVar RCV Id:
RCV000854238
dbSNP Id:
rs386829041
MyVariant Identifiers:
chrMT:g.8563A>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.8563A>G , J01415.2:m.8563A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361851.1:c.198A>G
(MT-ATP8)
ENSP00000355265.1:p.Pro66=
ENST00000361899.2:c.37A>G
(MT-ATP6)
ENSP00000354632.2:p.Thr13Ala
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