Canonical Allele Identifier: CA16603284
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 377154
ClinVar RCV Id: RCV000444831
dbSNP Id: rs28357370
MyVariant Identifiers: chrMT:g.15487A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15487A>G , J01415.2:m.15487A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.741A>G ENSP00000354554.2:p.Pro247=
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