Canonical Allele Identifier: CA337099972
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693699
ClinVar RCV Id: RCV000855079
dbSNP Id: rs202227543
MyVariant Identifiers: chrMT:g.14258G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14258G>A , J01415.2:m.14258G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.416C>T ENSP00000354665.2:p.Pro139Leu
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