Canonical Allele Identifier: CA414807575

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 693331
• ClinVar RCV Id: RCV000854694
• dbSNP Id: rs1603223028
• MyVariant Identifiers: chrMT:g.10932C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10932C>T , J01415.2:m.10932C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.173C>T	ENSP00000354961.2:p.Ser58Phe