Canonical Allele Identifier: CA913173224
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693838
ClinVar RCV Id: RCV000855238
dbSNP Id: rs1603225142

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15200G>A , J01415.2:m.15200G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.454G>A ENSP00000354554.2:p.Ala152Thr