Canonical Allele Identifier: CA414818884
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693583
ClinVar RCV Id: RCV000854960
dbSNP Id: rs1603224281
MyVariant Identifiers: chrMT:g.13645T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13645T>A , J01415.2:m.13645T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1309T>A ENSP00000354813.2:p.Phe437Ile
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