Canonical Allele Identifier: CA645611444
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693799
ClinVar RCV Id: RCV000855194
dbSNP Id: rs1603224995
COSMIC: COSM1138288 COSM1138289
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14973G>A , J01415.2:m.14973G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.227G>A ENSP00000354554.2:p.Gly76Asp
Search 100 bp 5'
Search 100 bp 3'