ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA337098340
Gene: MT-CO3
HGNC
NCBI
Linked Data
dbSNP:
2853824
MyVariant.info:
GRCh38
chrMT:g.9347A>G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.9347A>G , J01415.2:m.9347A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000362079.2:c.141A>G
ENSP00000354982.2:p.Leu47=
Search 100 bp 5'
Search 100 bp 3'