Canonical Allele Identifier: CA414805098
Gene: MT-ND3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10339T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10339T>C , J01415.2:m.10339T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.281T>C ENSP00000355206.2:p.Leu94Ser