Canonical Allele Identifier: CA120638
Gene:

Linked Data

ClinVar Variation Id: 9713
dbSNP Id: rs2853826
MyVariant Identifiers: chrMT:g.10398A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10398A>G , J01415.2:m.10398A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:n.340A>G ENSP00000355206.2:p.Thr114Ala