Canonical Allele Identifier: CA16040641

Gene: MT-CYB

Linked Data

• ClinVar Variation Id: 370064
• ClinVar RCV Id: RCV000408922 ; RCV000408942
• dbSNP Id: rs1057516074
• MyVariant Identifiers: chrMT:g.15127C>T (hg38)
• PubMed: PMID:28027978

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15127C>T , J01415.2:m.15127C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000361789.2:c.381C>T	ENSP00000354554.2:p.Ala127=