Canonical Allele Identifier: CA414820636
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693653
ClinVar RCV Id: RCV000855033
dbSNP Id: rs1603224484
MyVariant Identifiers: chrMT:g.14041C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14041C>T , J01415.2:m.14041C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1705C>T ENSP00000354813.2:p.His569Tyr
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