Canonical Allele Identifier: CA414820740
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693663
ClinVar RCV Id: RCV000855043
dbSNP Id: rs1556424379
MyVariant Identifiers: chrMT:g.14063T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14063T>C , J01415.2:m.14063T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1727T>C ENSP00000354813.2:p.Ile576Thr
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