Canonical Allele Identifier: CA414822590
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693725
ClinVar RCV Id: RCV000855110
dbSNP Id: rs1603224737
MyVariant Identifiers: chrMT:g.14462G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14462G>A , J01415.2:m.14462G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.212C>T ENSP00000354665.2:p.Thr71Ile
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