Canonical Allele Identifier: CA414809586

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 693349
• ClinVar RCV Id: RCV000854713
• dbSNP Id: rs1603223138
• MyVariant Identifiers: chrMT:g.11157T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11157T>C , J01415.2:m.11157T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.398T>C	ENSP00000354961.2:p.Ile133Thr