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Canonical Allele Identifier:
CA414793459
Gene: MT-CO2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
692767
ClinVar RCV Id:
RCV000854094
RCV000992350
RCV003319215
dbSNP Id:
rs1553139599
MyVariant Identifiers:
chrMT:g.7724A>T (hg38)
ERepo:
CA414793459/MONDO:0044970/014
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.7724A>T , J01415.2:m.7724A>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361739.1:c.139A>T
ENSP00000354876.1:p.Thr47Ser
Search 100 bp 5'
Search 100 bp 3'