Canonical Allele Identifier: CA414780619
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 585066
dbSNP Id: rs1569484003
MyVariant Identifiers: chrMT:g.5505A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5505A>G , J01415.2:m.5505A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.1036A>G ENSP00000355046.4:p.Ile346Val