Canonical Allele Identifier: CA414775046
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692469
ClinVar RCV Id: RCV000853784
dbSNP Id: rs1603219530
MyVariant Identifiers: chrMT:g.4632G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4632G>A , J01415.2:m.4632G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.163G>A ENSP00000355046.4:p.Ala55Thr
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