Canonical Allele Identifier: CA414810772
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.11702C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11702C>T , J01415.2:m.11702C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.943C>T ENSP00000354961.2:p.Leu315Phe
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