Canonical Allele Identifier: CA414779707
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692567
dbSNP Id: rs28690990
MyVariant Identifiers: chrMT:g.5293G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5293G>A , J01415.2:m.5293G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.824G>A ENSP00000355046.4:p.Ser275Asn