Canonical Allele Identifier: CA337099365
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs2853497
MyVariant Identifiers: chrMT:g.12007G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12007G>A , J01415.2:m.12007G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:n.1248G>A ENSP00000354961.2:p.Trp416Ter