Canonical Allele Identifier: CA16603354

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 377369
• ClinVar RCV Id: RCV000426856 ; RCV000855387 ; RCV003319197
• dbSNP Id: rs1057520206
• MyVariant Identifiers: chrMT:g.15848A>G (hg38)
• ERepo: CA16603354/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15848A>G , J01415.2:m.15848A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.1102A>G	ENSP00000354554.2:p.Thr368Ala