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

Linked Data

ClinVar Variation Id: 439912
ClinVar RCV Id: RCV000506977 RCV000854079 RCV003319204
dbSNP Id: rs1556423314
MyVariant Identifiers: chrMT:g.7637G>A (hg38)
ERepo: CA414793083/MONDO:0044970/014
JSON-LD

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
Search 100 bp 5'
Search 100 bp 3'