Canonical Allele Identifier: CA337098828

Gene: MT-ND3

Linked Data

• ClinVar Variation Id: 693290
• ClinVar RCV Id: RCV000854650
• dbSNP Id: rs28719882
• MyVariant Identifiers: chrMT:g.10401G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10401G>A , J01415.2:m.10401G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000361227.2:c.343G>A	ENSP00000355206.2:p.Glu115Lys