Canonical Allele Identifier: CA337099752
Gene: MT-ND5 HGNC NCBI

Linked Data

dbSNP Id: rs28439808
MyVariant Identifiers: chrMT:g.13609C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13609C>G , J01415.2:m.13609C>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1273C>G ENSP00000354813.2:p.Arg425Gly