Canonical Allele Identifier: CA414823009

Gene: MT-ND6

Linked Data

• ClinVar Variation Id: 693734
• ClinVar RCV Id: RCV000855121
• dbSNP Id: rs1556424459
• MyVariant Identifiers: chrMT:g.14552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14552A>G , J01415.2:m.14552A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361681.2:c.122T>C	ENSP00000354665.2:p.Val41Ala