ClinGen Allele Registry
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Canonical Allele Identifier:
CA414772659
Gene: MT-ND1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
692346
ClinVar RCV Id:
RCV000853646
dbSNP Id:
rs1603218926
COSMIC:
COSM1599865
COSM1599866
MyVariant Identifiers:
chrMT:g.3380G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.3380G>A , J01415.2:m.3380G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361390.2:c.74G>A
ENSP00000354687.2:p.Arg25Gln
Search 100 bp 5'
Search 100 bp 3'