Canonical Allele Identifier: CA414821320
Gene: MT-ND6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.14192A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14192A>C , J01415.2:m.14192A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.482T>G ENSP00000354665.2:p.Phe161Cys