Canonical Allele Identifier: CA337096925
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692471
ClinVar RCV Id: RCV000853786
dbSNP Id: rs41510547
MyVariant Identifiers: chrMT:g.4639T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4639T>C , J01415.2:m.4639T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.170T>C ENSP00000355046.4:p.Ile57Thr
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