Canonical Allele Identifier: CA913174965
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693962
ClinVar RCV Id: RCV000855384
dbSNP Id: rs1603225529

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15831T>C , J01415.2:m.15831T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1085T>C ENSP00000354554.2:p.Ile362Thr