Canonical Allele Identifier: CA414793083
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439912
dbSNP Id: rs1556423314
MyVariant Identifiers: chrMT:g.7637G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7637G>A , J01415.2:m.7637G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.52G>A ENSP00000354876.1:p.Glu18Lys