Canonical Allele Identifier: CA414775317
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692479
ClinVar RCV Id: RCV000853795
dbSNP Id: rs1603219555
MyVariant Identifiers: chrMT:g.4689A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4689A>G , J01415.2:m.4689A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.220A>G ENSP00000355046.4:p.Ile74Val
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