Canonical Allele Identifier: CA414823214
Gene: MT-ND6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.14598T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14598T>A , J01415.2:m.14598T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.76A>T ENSP00000354665.2:p.Ile26Phe