Canonical Allele Identifier: CA414813765

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693465
• ClinVar RCV Id: RCV000854837
• dbSNP Id: rs28759201
• MyVariant Identifiers: chrMT:g.12561G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12561G>C , J01415.2:m.12561G>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.225G>C	ENSP00000354813.2:p.Gln75His