Canonical Allele Identifier: CA414774671
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692459
ClinVar RCV Id: RCV000853774
dbSNP Id: rs1603219496
MyVariant Identifiers: chrMT:g.4531C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4531C>T , J01415.2:m.4531C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.62C>T ENSP00000355046.4:p.Ala21Val
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