Canonical Allele Identifier: CA120632
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 9702
dbSNP Id: rs267606897
MyVariant Identifiers: chrMT:g.13513G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13513G>A , J01415.2:m.13513G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1177G>A ENSP00000354813.2:p.Asp393Asn