Canonical Allele Identifier: CA414773132
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692377
ClinVar RCV Id: RCV000853683
dbSNP Id: rs1556422761
MyVariant Identifiers: chrMT:g.3607G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3607G>A , J01415.2:m.3607G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.301G>A ENSP00000354687.2:p.Gly101Ser