Canonical Allele Identifier: CA337099941
Gene: MT-ND6 HGNC NCBI
ClinVar RCV:
RCV000855062
ClinVar Variation:
693682
dbSNP:
28357671
MyVariant.info:
GRCh38 chrMT:g.14178T>C
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14178T>C , J01415.2:m.14178T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.496A>G ENSP00000354665.2:p.Ile166Val
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