Canonical Allele Identifier: CA337097884
Gene: MT-ATP8 HGNC NCBI

Linked Data

dbSNP Id: rs1116907
MyVariant Identifiers: chrMT:g.8468C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8468C>T , J01415.2:m.8468C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.103C>T ENSP00000355265.1:p.Leu35=