Canonical Allele Identifier: CA913173140
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 1684906
ClinVar RCV Id: RCV002247998
dbSNP Id: rs2124598725
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15170G>A , J01415.2:m.15170G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.424G>A ENSP00000354554.2:p.Gly142Arg
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