Canonical Allele Identifier: CA414780461
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692593
ClinVar RCV Id: RCV000853911
dbSNP Id: rs1603219973
MyVariant Identifiers: chrMT:g.5466A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5466A>G , J01415.2:m.5466A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.997A>G ENSP00000355046.4:p.Thr333Ala