Canonical Allele Identifier: CA645509242

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 374216
• ClinVar RCV Id: RCV000509010
• dbSNP Id: rs1556424489
• MyVariant Identifiers: chrMT:g.14771C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14771C>A , J01415.2:m.14771C>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.25C>A	ENSP00000354554.2:p.Pro9Thr