Canonical Allele Identifier: CA414807713
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10965C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10965C>A , J01415.2:m.10965C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.206C>A ENSP00000354961.2:p.Thr69Asn