Canonical Allele Identifier: CA414775263
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692476
ClinVar RCV Id: RCV000853792
dbSNP Id: rs1556422884
MyVariant Identifiers: chrMT:g.4674A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4674A>G , J01415.2:m.4674A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.205A>G ENSP00000355046.4:p.Ile69Val
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