ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA345705
Gene: MT-CYB
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.15043G>A
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000128804
RCV003886378
ClinVar Variation:
140589
dbSNP:
193302985
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.15043G>A , J01415.2:m.15043G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361789.2:c.297G>A
ENSP00000354554.2:p.Gly99=
Search 100 bp 5'
Search 100 bp 3'