Canonical Allele Identifier: CA414813696
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693461
ClinVar RCV Id: RCV000854833
dbSNP Id: rs1603223799
MyVariant Identifiers: chrMT:g.12545C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12545C>T , J01415.2:m.12545C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.209C>T ENSP00000354813.2:p.Thr70Ile
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