Canonical Allele Identifier: CA414774152
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692421
ClinVar RCV Id: RCV000853731
dbSNP Id: rs1603219293
MyVariant Identifiers: chrMT:g.4084G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4084G>A , J01415.2:m.4084G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.778G>A ENSP00000354687.2:p.Val260Ile
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