Canonical Allele Identifier: CA170522

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 143875
• ClinVar RCV Id: RCV000133414 ; RCV000855222
• dbSNP Id: rs527236172
• MyVariant Identifiers: chrMT:g.15098A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15098A>G , J01415.2:m.15098A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.352A>G	ENSP00000354554.2:p.Ile118Val