Canonical Allele Identifier: CA345757
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143919
ClinVar RCV Id: RCV000133450
dbSNP Id: rs193302983
MyVariant Identifiers: chrMT:g.14905G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14905G>A , J01415.2:m.14905G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.159G>A ENSP00000354554.2:p.Met53Ile