Canonical Allele Identifier: CA120624
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9686
ClinVar RCV Id: RCV000010324 RCV003985259
dbSNP Id: rs207460005
MyVariant Identifiers: chrMT:g.14787_14790del (hg38)
PubMed: PMID:9894888
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14787_14790del , J01415.2:m.14787_14790del GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.41_44del ENSP00000354554.2:p.Ile14ThrfsTer27
Search 100 bp 5'
Search 100 bp 3'