Canonical Allele Identifier: CA414775286
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692478
ClinVar RCV Id: RCV000853794
dbSNP Id: rs1603219554
MyVariant Identifiers: chrMT:g.4680C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4680C>A , J01415.2:m.4680C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.211C>A ENSP00000355046.4:p.Leu71Ile
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