Canonical Allele Identifier: CA414814515
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693478
ClinVar RCV Id: RCV000854850
dbSNP Id: rs1603223875
MyVariant Identifiers: chrMT:g.12715A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12715A>G , J01415.2:m.12715A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.379A>G ENSP00000354813.2:p.Thr127Ala