Canonical Allele Identifier: CA414822609
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693727
ClinVar RCV Id: RCV000855112
dbSNP Id: rs1603224741
MyVariant Identifiers: chrMT:g.14466T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14466T>C , J01415.2:m.14466T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.208A>G ENSP00000354665.2:p.Thr70Ala