Canonical Allele Identifier: CA337099453
Gene: MT-ND5 HGNC NCBI

Linked Data

dbSNP Id: rs879025446
MyVariant Identifiers: chrMT:g.12348C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12348C>T , J01415.2:m.12348C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.12C>T ENSP00000354813.2:p.His4=