Canonical Allele Identifier: CA414809574

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 693348
• ClinVar RCV Id: RCV000854712
• dbSNP Id: rs1556423903
• MyVariant Identifiers: chrMT:g.11151C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11151C>T , J01415.2:m.11151C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.392C>T	ENSP00000354961.2:p.Ala131Val