ClinGen Allele Registry
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Canonical Allele Identifier:
CA414795702
Gene: MT-CO2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
692829
ClinVar RCV Id:
RCV000854157
dbSNP Id:
rs1603221351
MyVariant Identifiers:
chrMT:g.8252C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.8252C>T , J01415.2:m.8252C>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361739.1:c.667C>T
ENSP00000354876.1:p.Pro223Ser
Search 100 bp 5'
Search 100 bp 3'