Canonical Allele Identifier: CA414819221
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13721T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13721T>C , J01415.2:m.13721T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1385T>C ENSP00000354813.2:p.Leu462Pro