Canonical Allele Identifier: CA414814112
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693472
ClinVar RCV Id: RCV000854844
dbSNP Id: rs1556424136
MyVariant Identifiers: chrMT:g.12634A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12634A>G , J01415.2:m.12634A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.298A>G ENSP00000354813.2:p.Ile100Val
Search 100 bp 5'
Search 100 bp 3'