Canonical Allele Identifier: CA913172133
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693769
ClinVar RCV Id: RCV000855160
dbSNP Id: rs1603224902

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14804G>A , J01415.2:m.14804G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.58G>A ENSP00000354554.2:p.Asp20Asn