ClinGen Allele Registry
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Canonical Allele Identifier:
CA414809522
Gene: MT-ND4
HGNC
NCBI
Linked Data
dbSNP Id:
rs1603223119
COSMIC:
COSM1138226
MyVariant Identifiers:
chrMT:g.11126G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.11126G>A , J01415.2:m.11126G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361381.2:c.367G>A
ENSP00000354961.2:p.Glu123Lys
Search 100 bp 5'
Search 100 bp 3'