ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA414803388
Gene: MT-CO3
HGNC
NCBI
Linked Data
dbSNP Id:
rs2068717814
MyVariant Identifiers:
chrMT:g.9644A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.9644A>G , J01415.2:m.9644A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000362079.2:c.438A>G
ENSP00000354982.2:p.Ter146Trp
Search 100 bp 5'
Search 100 bp 3'