Canonical Allele Identifier: CA414772929
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692362
ClinVar RCV Id: RCV000853667
dbSNP Id: rs1603218990
MyVariant Identifiers: chrMT:g.3508A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3508A>G , J01415.2:m.3508A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.202A>G ENSP00000354687.2:p.Ile68Val
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