Allele Registry

Canonical Allele Identifier: CA337100791

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.16230A>G

Linked Data - NCBI & NCI

ClinVar Allele:

1517319

ClinVar RCV:

RCV002037091

ClinVar Variation:

1525975

dbSNP:

2853514

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.16230A>G , J01415.2:m.16230A>G	GRCh38

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