Canonical Allele Identifier: CA414817990

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693554
• ClinVar RCV Id: RCV000854929
• dbSNP Id: rs1603224188
• MyVariant Identifiers: chrMT:g.13436C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13436C>A , J01415.2:m.13436C>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1100C>A	ENSP00000354813.2:p.Pro367His