Canonical Allele Identifier: CA414814016
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693469
ClinVar RCV Id: RCV000854841
dbSNP Id: rs1603223834
MyVariant Identifiers: chrMT:g.12613G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12613G>T , J01415.2:m.12613G>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.277G>T ENSP00000354813.2:p.Ala93Ser