Canonical Allele Identifier: CA414822695

Gene: MT-ND6

Linked Data

• ClinVar Variation Id: 693729
• ClinVar RCV Id: RCV000855114
• dbSNP Id: rs199476104
• MyVariant Identifiers: chrMT:g.14484T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000361681.2:c.190A>C	ENSP00000354665.2:p.Met64Leu