Canonical Allele Identifier: CA340939
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 9708
dbSNP Id: rs199476112
MyVariant Identifiers: chrMT:g.11778G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11778G>A , J01415.2:m.11778G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1019G>A ENSP00000354961.2:p.Arg340His