Canonical Allele Identifier: CA414819258
Gene: MT-ND5 HGNC NCBI

Linked Data

dbSNP Id: rs1556424316
MyVariant Identifiers: chrMT:g.13729G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13729G>A , J01415.2:m.13729G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1393G>A ENSP00000354813.2:p.Gly465Arg