ClinGen Allele Registry
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Canonical Allele Identifier:
CA414773722
Gene: MT-ND1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.3882G>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.3882G>C , J01415.2:m.3882G>C
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361390.2:c.576G>C
ENSP00000354687.2:p.Glu192Asp
Search 100 bp 5'
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