ClinGen Allele Registry
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Canonical Allele Identifier:
CA414814095
Gene: MT-ND5
HGNC
NCBI
Linked Data
COSMIC:
COSM488732
MyVariant Identifiers:
chrMT:g.12630G>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.12630G>C , J01415.2:m.12630G>C
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361567.2:c.294G>C
ENSP00000354813.2:p.Trp98Cys
Search 100 bp 5'
Search 100 bp 3'