ClinGen Allele Registry
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Canonical Allele Identifier:
CA337098946
Gene: MT-ND4L
HGNC
NCBI
Linked Data
dbSNP Id:
rs879190069
MyVariant Identifiers:
chrMT:g.10670C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.10670C>T , J01415.2:m.10670C>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361335.1:c.201C>T
ENSP00000354728.1:p.Ala67=
Search 100 bp 5'
Search 100 bp 3'