Canonical Allele Identifier: CA414807405
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693322
ClinVar RCV Id: RCV000854684
dbSNP Id: rs1603223008
MyVariant Identifiers: chrMT:g.10895A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10895A>G , J01415.2:m.10895A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.136A>G ENSP00000354961.2:p.Asn46Asp