Canonical Allele Identifier: CA10581273
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235315
ClinVar RCV Id: RCV000224714 RCV000853750
dbSNP Id: rs878853008
MyVariant Identifiers: chrMT:g.4219G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4219G>A , J01415.2:m.4219G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.913G>A ENSP00000354687.2:p.Val305Ile
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