Canonical Allele Identifier: CA414774598
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692451
ClinVar RCV Id: RCV000853766
dbSNP Id: rs1603219482
MyVariant Identifiers: chrMT:g.4497T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4497T>C , J01415.2:m.4497T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.28T>C ENSP00000355046.4:p.Tyr10His
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