Canonical Allele Identifier: CA414820643
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693654
ClinVar RCV Id: RCV000855034
dbSNP Id: rs1603224485
MyVariant Identifiers: chrMT:g.14042A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14042A>T , J01415.2:m.14042A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1706A>T ENSP00000354813.2:p.His569Leu
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