Allele Registry

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Canonical Allele Identifier: CA414811721

Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693385

ClinVar RCV Id: RCV000854753

dbSNP Id: rs1569484466

COSMIC: COSM1138239 COSM1138240

MyVariant Identifiers: chrMT:g.11928A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11928A>G , J01415.2:m.11928A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.1169A>G	ENSP00000354961.2:p.Asn390Ser

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