Canonical Allele Identifier: CA337100378

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 693874
• ClinVar RCV Id: RCV000855281
• dbSNP Id: rs199721378
• MyVariant Identifiers: chrMT:g.15381C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15381C>T , J01415.2:m.15381C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.635C>T	ENSP00000354554.2:p.Thr212Ile