Canonical Allele Identifier: CA414818755

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693579
• ClinVar RCV Id: RCV000854955
• dbSNP Id: rs1603224262
• MyVariant Identifiers: chrMT:g.13612A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13612A>T , J01415.2:m.13612A>T	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000361567.2:c.1276A>T	ENSP00000354813.2:p.Ile426Leu