Canonical Allele Identifier: CA337099911
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693660
ClinVar RCV Id: RCV000855040
dbSNP Id: rs878865648
MyVariant Identifiers: chrMT:g.14059A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14059A>G , J01415.2:m.14059A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1723A>G ENSP00000354813.2:p.Ile575Val
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