Canonical Allele Identifier: CA10581194
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 235010
ClinVar RCV Id: RCV000223843 RCV000854830
dbSNP Id: rs876661356
MyVariant Identifiers: chrMT:g.12535C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12535C>T , J01415.2:m.12535C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.199C>T ENSP00000354813.2:p.His67Tyr
Search 100 bp 5'
Search 100 bp 3'