Allele Registry

Canonical Allele Identifier: CA340925

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.8361G>A

Linked Data - NCBI & NCI

ClinVar Allele:

24624

ClinVar RCV:

RCV000010202

ClinVar Variation:

9585

dbSNP:

118192104

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8361G>A , J01415.2:m.8361G>A	GRCh38

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