Canonical Allele Identifier: CA414802436
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693125
ClinVar RCV Id: RCV000854476
dbSNP Id: rs1556423633
MyVariant Identifiers: chrMT:g.9210A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9210A>G , J01415.2:m.9210A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.4A>G ENSP00000354982.2:p.Thr2Ala
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Search 100 bp 3'