Canonical Allele Identifier: CA120578
Gene:

Linked Data

ClinVar Variation Id: 9613
ClinVar RCV Id: RCV000010237 RCV000850986
dbSNP Id: rs41362547
MyVariant Identifiers: chrMT:g.10044A>G (hg38)
PubMed: PMID:8888049 PMID:12621050
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10044A>G , J01415.2:m.10044A>G GRCh38
Search 100 bp 5'
Search 100 bp 3'