Canonical Allele Identifier: CA345761
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143927
ClinVar RCV Id: RCV000133458
dbSNP Id: rs193302997
MyVariant Identifiers: chrMT:g.15670T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15670T>C , J01415.2:m.15670T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.924T>C ENSP00000354554.2:p.His308=