Canonical Allele Identifier: CA337099798
Gene: MT-ND5 HGNC NCBI

Linked Data

dbSNP Id: rs368357802
MyVariant Identifiers: chrMT:g.13755C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13755C>T , J01415.2:m.13755C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1419C>T ENSP00000354813.2:p.Ser473=