Canonical Allele Identifier: CA10581323
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 235471
ClinVar RCV Id: RCV000224379
dbSNP Id: rs878853046
MyVariant Identifiers: chrMT:g.12432C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12432C>T , J01415.2:m.12432C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.96C>T ENSP00000354813.2:p.Tyr32=