Canonical Allele Identifier: CA414793385
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692764
ClinVar RCV Id: RCV000854091
dbSNP Id: rs1556423333
MyVariant Identifiers: chrMT:g.7706G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7706G>A , J01415.2:m.7706G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.121G>A ENSP00000354876.1:p.Ala41Thr
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Search 100 bp 3'