Canonical Allele Identifier: CA337100215
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693791
ClinVar RCV Id: RCV000855185
dbSNP Id: rs201551481
MyVariant Identifiers: chrMT:g.14927A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14927A>G , J01415.2:m.14927A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.181A>G ENSP00000354554.2:p.Thr61Ala