Allele Registry

Canonical Allele Identifier: CA337095938

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.750A>G

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000509422

RCV003886405

ClinVar Variation:

441148

dbSNP:

2853518

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.750A>G , J01415.2:m.750A>G	GRCh38

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