Canonical Allele Identifier: CA254859
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9726
ClinVar RCV Id: RCV000010376 RCV000010377 RCV000853653
dbSNP Id: rs199476120
MyVariant Identifiers: chrMT:g.3397A>G (hg38)
PubMed: PMID:7624338
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3397A>G , J01415.2:m.3397A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.91A>G ENSP00000354687.2:p.Ile31Val
Search 100 bp 5'
Search 100 bp 3'