Canonical Allele Identifier: CA414821017
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693669
ClinVar RCV Id: RCV000855049
dbSNP Id: rs1603224535
MyVariant Identifiers: chrMT:g.14122A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14122A>G , J01415.2:m.14122A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1786A>G ENSP00000354813.2:p.Ile596Val