Canonical Allele Identifier: CA10581339
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 235516
ClinVar RCV Id: RCV000224763
dbSNP Id: rs878853056
MyVariant Identifiers: chrMT:g.4688T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4688T>C , J01415.2:m.4688T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.219T>C ENSP00000355046.4:p.Ala73=
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