Canonical Allele Identifier: CA414781587
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692618
ClinVar RCV Id: RCV000853937
dbSNP Id: rs1603220261
MyVariant Identifiers: chrMT:g.6081G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6081G>T , J01415.2:m.6081G>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.178G>T ENSP00000354499.2:p.Ala60Ser
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Search 100 bp 3'