Canonical Allele Identifier: CA414805411

Gene: MT-ND3

Linked Data

• ClinVar Variation Id: 693288
• ClinVar RCV Id: RCV000854648
• dbSNP Id: rs2853826
• MyVariant Identifiers: chrMT:g.10398A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10398A>T , J01415.2:m.10398A>T	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000361227.2:c.340A>T	ENSP00000355206.2:p.Thr114Ser