Canonical Allele Identifier: CA270620
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143896
dbSNP Id: rs527236191
MyVariant Identifiers: chrMT:g.15649A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15649A>G , J01415.2:m.15649A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.903A>G ENSP00000354554.2:p.Leu301=