Canonical Allele Identifier: CA414814201
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.12652T>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12652T= , J01415.2:m.12652T= GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.316T= ENSP00000354813.2:p.Ter106=
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