Canonical Allele Identifier: CA170535
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143921
ClinVar RCV Id: RCV000133452
dbSNP Id: rs527236205
COSMIC: COSM1155587 COSM1155588
MyVariant Identifiers: chrMT:g.15061A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15061A>G , J01415.2:m.15061A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.315A>G ENSP00000354554.2:p.Gly105=
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