Canonical Allele Identifier: CA16603348
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 377340
dbSNP Id: rs1057520201
MyVariant Identifiers: chrMT:g.4132G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4132G>A , J01415.2:m.4132G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.826G>A ENSP00000354687.2:p.Ala276Thr