Canonical Allele Identifier: CA414820683

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693656
• ClinVar RCV Id: RCV000855036
• dbSNP Id: rs879112261
• MyVariant Identifiers: chrMT:g.14050T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14050T>C , J01415.2:m.14050T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1714T>C	ENSP00000354813.2:p.Ser572Pro