Canonical Allele Identifier: CA170520

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 143866
• ClinVar RCV Id: RCV000133405 ; RCV002247517
• dbSNP Id: rs527236163
• MyVariant Identifiers: chrMT:g.14784T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14784T>C , J01415.2:m.14784T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.38T>C	ENSP00000354554.2:p.Leu13Ser