Allele Registry

Canonical Allele Identifier: CA131006

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.1438A>G

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000035045

RCV000509092

ClinVar Variation:

42220

dbSNP:

2001030

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1438A>G , J01415.2:m.1438A>G	GRCh38

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