ClinGen Allele Registry
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Canonical Allele Identifier:
CA414809579
Gene: MT-ND4
HGNC
NCBI
Linked Data
dbSNP Id:
rs1603223136
MyVariant Identifiers:
chrMT:g.11154T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.11154T>C , J01415.2:m.11154T>C
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361381.2:c.395T>C
ENSP00000354961.2:p.Ile132Thr
Search 100 bp 5'
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