Canonical Allele Identifier: CA337099036
Gene:

Linked Data

dbSNP Id: rs2857284
MyVariant Identifiers: chrMT:g.10873T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10873T>C , J01415.2:m.10873T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:n.114T>C ENSP00000354961.2:p.Pro38=