Canonical Allele Identifier: CA345916
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 155887
ClinVar RCV Id: RCV000144012
dbSNP Id: rs587776438
MyVariant Identifiers: chrMT:g.10254G>A (hg38)
PubMed: PMID:20202874 PMID:20301352
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10254G>A , J01415.2:m.10254G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.196G>A ENSP00000355206.2:p.Asp66Asn
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