Canonical Allele Identifier: CA414821837
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693705
ClinVar RCV Id: RCV000855086
dbSNP Id: rs1603224659
MyVariant Identifiers: chrMT:g.14301T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14301T>C , J01415.2:m.14301T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.373A>G ENSP00000354665.2:p.Ile125Val
Search 100 bp 5'
Search 100 bp 3'