Canonical Allele Identifier: CA414809506

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 693343
• ClinVar RCV Id: RCV000854707
• dbSNP Id: rs1603223116
• MyVariant Identifiers: chrMT:g.11120T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11120T>C , J01415.2:m.11120T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.361T>C	ENSP00000354961.2:p.Phe121Leu