Allele Registry

Canonical Allele Identifier: CA250584

Gene: MT-CO1 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.6264G>A

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000010305

RCV000853954

ClinVar Variation:

9667

dbSNP:

267606882

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.6264G>A , J01415.2:m.6264G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361624.2:c.361G>A	ENSP00000354499.2:p.Gly121Arg

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