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
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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
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Search 100 bp 3'