Canonical Allele Identifier: CA414807782
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10979C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10979C>T , J01415.2:m.10979C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.220C>T ENSP00000354961.2:p.Pro74Ser
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