Canonical Allele Identifier: CA337099854
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693636
ClinVar RCV Id: RCV000855014
dbSNP Id: rs28359184
MyVariant Identifiers: chrMT:g.13928G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13928G>A , J01415.2:m.13928G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1592G>A ENSP00000354813.2:p.Ser531Asn