Canonical Allele Identifier: CA658653728

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 441132
• ClinVar RCV Id: RCV000509193
• dbSNP Id: rs1556424593
• MyVariant Identifiers: chrMT:g.15492T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15492T>C , J01415.2:m.15492T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.746T>C	ENSP00000354554.2:p.Leu249Pro