Canonical Allele Identifier: CA414818952
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13660A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13660A>C , J01415.2:m.13660A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1324A>C ENSP00000354813.2:p.Asn442His
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