Canonical Allele Identifier: CA414774335
Gene: MT-ND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4169T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4169T>A , J01415.2:m.4169T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.863T>A ENSP00000354687.2:p.Leu288His
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