Allele Registry

Canonical Allele Identifier: CA254857

Gene: MT-ND4 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.11084A>G

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000010355

RCV000854703

ClinVar Variation:

9709

dbSNP:

199476113

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11084A>G , J01415.2:m.11084A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.325A>G	ENSP00000354961.2:p.Thr109Ala

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