Canonical Allele Identifier: CA913174845
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693953
ClinVar RCV Id: RCV000855374
dbSNP Id: rs1556424663

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15789C>T , J01415.2:m.15789C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1043C>T ENSP00000354554.2:p.Thr348Ile