Canonical Allele Identifier: CA414823110

Gene: MT-ND6

Linked Data

• ClinVar Variation Id: 693740
• ClinVar RCV Id: RCV000855127
• dbSNP Id: rs386829218
• MyVariant Identifiers: chrMT:g.14574C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14574C>T , J01415.2:m.14574C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361681.2:c.100G>A	ENSP00000354665.2:p.Val34Ile