Canonical Allele Identifier: CA414822830
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693730
ClinVar RCV Id: RCV000855117
dbSNP Id: rs1603224772
MyVariant Identifiers: chrMT:g.14514T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14514T>C , J01415.2:m.14514T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.160A>G ENSP00000354665.2:p.Ile54Val
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