Canonical Allele Identifier: CA645611459
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693871
ClinVar RCV Id: RCV000855278
dbSNP Id: rs1603225244

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15357G>A , J01415.2:m.15357G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.611G>A ENSP00000354554.2:p.Gly204Glu