ClinGen Allele Registry
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Canonical Allele Identifier:
CA414772675
Gene: MT-ND1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1569483877
MyVariant Identifiers:
chrMT:g.3387T>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.3387T>G , J01415.2:m.3387T>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361390.2:c.81T>G
ENSP00000354687.2:p.Ile27Met
Search 100 bp 5'
Search 100 bp 3'