Canonical Allele Identifier: CA337099193
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 522716
ClinVar RCV Id: RCV000625869
dbSNP Id: rs2853493
MyVariant Identifiers: chrMT:g.11467A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11467A>G , J01415.2:m.11467A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:n.708A>G ENSP00000354961.2:p.Leu236=