Canonical Allele Identifier: CA16040647
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 370047
ClinVar RCV Id: RCV000408951
dbSNP Id: rs1057516059
MyVariant Identifiers: chrMT:g.4664C>T (hg38)
PubMed: PMID:28027978
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4664C>T , J01415.2:m.4664C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.195C>T ENSP00000355046.4:p.Thr65=
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