Canonical Allele Identifier: CA414775478
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4719T>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4719T= , J01415.2:m.4719T= GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.250T= ENSP00000355046.4:p.Ter84=
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