Allele Registry

Canonical Allele Identifier: CA337096419

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.3010G>A

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000509285

ClinVar Variation:

441149

dbSNP:

3928306

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3010G>A , J01415.2:m.3010G>A	GRCh38

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