Canonical Allele Identifier: CA170532
Gene:

Linked Data

ClinVar Variation Id: 143903
ClinVar RCV Id: RCV000133442 RCV000851132
dbSNP Id: rs527236198
MyVariant Identifiers: chrMT:g.15928G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15928G>A , J01415.2:m.15928G>A GRCh38
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