Canonical Allele Identifier: CA414823276
Gene: MT-ND6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.14613A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14613A>T , J01415.2:m.14613A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.61T>A ENSP00000354665.2:p.Ser21Thr
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