Canonical Allele Identifier: CA414774577
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4487A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4487A>C , J01415.2:m.4487A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.18A>C ENSP00000355046.4:p.Gln6His
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