ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA414793913
Gene: MT-CO2
HGNC
NCBI
Linked Data
dbSNP Id:
rs1603221167
MyVariant Identifiers:
chrMT:g.7832A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.7832A>G , J01415.2:m.7832A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361739.1:c.247A>G
ENSP00000354876.1:p.Ile83Val
Search 100 bp 5'
Search 100 bp 3'