Canonical Allele Identifier: CA414822170
Gene: MT-ND6 HGNC NCBI

Linked Data

dbSNP Id: rs386829210
MyVariant Identifiers: chrMT:g.14371T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14371T>C , J01415.2:m.14371T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.303A>G ENSP00000354665.2:p.Gly101=
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