Canonical Allele Identifier: CA414819408
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693602
ClinVar RCV Id: RCV000854980
dbSNP Id: rs879154715
MyVariant Identifiers: chrMT:g.13762T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13762T>A , J01415.2:m.13762T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1426T>A ENSP00000354813.2:p.Ser476Thr
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