Canonical Allele Identifier: CA10581397

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 235673
• ClinVar RCV Id: RCV000224580
• dbSNP Id: rs377109096
• MyVariant Identifiers: chrMT:g.11167A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11167A>G , J01415.2:m.11167A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.408A>G	ENSP00000354961.2:p.Ter136Trp