Canonical Allele Identifier: CA337096887
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692448
ClinVar RCV Id: RCV000853763
dbSNP Id: rs201172504
MyVariant Identifiers: chrMT:g.4491G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4491G>A , J01415.2:m.4491G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.22G>A ENSP00000355046.4:p.Val8Ile
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