Canonical Allele Identifier: CA344827
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65518
ClinVar RCV Id: RCV000055707 RCV002291214
dbSNP Id: rs397515507
MyVariant Identifiers: chrMT:g.3635G>A (hg38)
ERepo: CA344827/MONDO:0044970/014
PubMed: PMID:20301353
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3635G>A , J01415.2:m.3635G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.329G>A ENSP00000354687.2:p.Ser110Asn
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