Canonical Allele Identifier: CA414823505
Gene: MT-ND6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.14665A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14665A>T , J01415.2:m.14665A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.9T>A ENSP00000354665.2:p.Tyr3Ter