Canonical Allele Identifier: CA913172387
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693787
ClinVar RCV Id: RCV000855181
dbSNP Id: rs1603224957

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14895T>C , J01415.2:m.14895T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.149T>C ENSP00000354554.2:p.Phe50Ser