Canonical Allele Identifier: CA414823507
Gene: MT-ND6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.14666T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14666T>A , J01415.2:m.14666T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.8A>T ENSP00000354665.2:p.Tyr3Phe
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