Canonical Allele Identifier: CA337100321

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 693843
• ClinVar RCV Id: RCV000855243
• dbSNP Id: rs2853506
• MyVariant Identifiers: chrMT:g.15218A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15218A>G , J01415.2:m.15218A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.472A>G	ENSP00000354554.2:p.Thr158Ala