ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA414802443
Gene: MT-CO3
HGNC
NCBI
Linked Data
dbSNP Id:
rs1556423635
MyVariant Identifiers:
chrMT:g.9213C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.9213C>T , J01415.2:m.9213C>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000362079.2:c.7C>T
ENSP00000354982.2:p.His3Tyr
Search 100 bp 5'
Search 100 bp 3'