Canonical Allele Identifier: CA913174363
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693913
ClinVar RCV Id: RCV000855330
dbSNP Id: rs1603225376
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15614G>A , J01415.2:m.15614G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.868G>A ENSP00000354554.2:p.Gly290Ser
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