Canonical Allele Identifier: CA10586050
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 252456
dbSNP Id: rs28358585
MyVariant Identifiers: chrMT:g.3505A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3505A>G , J01415.2:m.3505A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.199A>G ENSP00000354687.2:p.Thr67Ala