Canonical Allele Identifier: CA10581197

Gene: MT-ND1

Linked Data

• ClinVar Variation Id: 235007
• ClinVar RCV Id: RCV000223871
• dbSNP Id: rs876661354
• MyVariant Identifiers: chrMT:g.3907G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3907G>A , J01415.2:m.3907G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361390.2:c.601G>A	ENSP00000354687.2:p.Ala201Thr