Canonical Allele Identifier: CA340932
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 9688
dbSNP Id: rs199476104
MyVariant Identifiers: chrMT:g.14484T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14484T>C , J01415.2:m.14484T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.190A>G ENSP00000354665.2:p.Met64Val