Canonical Allele Identifier: CA658653729

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 441130
• ClinVar RCV Id: RCV000509497
• dbSNP Id: rs1556424649
• MyVariant Identifiers: chrMT:g.15708G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15708G>A , J01415.2:m.15708G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.962G>A	ENSP00000354554.2:p.Ser321Asn