Canonical Allele Identifier: CA414823501
Gene: MT-ND6 HGNC NCBI

Linked Data

dbSNP Id: rs386829223
MyVariant Identifiers: chrMT:g.14664C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14664C>T , J01415.2:m.14664C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.10G>A ENSP00000354665.2:p.Ala4Thr
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