Canonical Allele Identifier: CA120618

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 9680
• ClinVar RCV Id: RCV000010318 ; RCV000855252
• dbSNP Id: rs207459999
• MyVariant Identifiers: chrMT:g.15242G>A (hg38)
• PubMed: PMID:11047755
• ERepo: CA120618/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15242G>A , J01415.2:m.15242G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.496G>A	ENSP00000354554.2:p.Gly166Arg