Canonical Allele Identifier: CA414774580
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692447
ClinVar RCV Id: RCV000853762
dbSNP Id: rs1603219476
MyVariant Identifiers: chrMT:g.4488C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4488C>T , J01415.2:m.4488C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.19C>T ENSP00000355046.4:p.Pro7Ser
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