Canonical Allele Identifier: CA120619
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9681
dbSNP Id: rs207460000
MyVariant Identifiers: chrMT:g.15150G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15150G>A , J01415.2:m.15150G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.404G>A ENSP00000354554.2:p.Ter135=