ClinGen Allele Registry
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Canonical Allele Identifier:
CA337096717
Gene: MT-ND1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
805048
ClinVar RCV Id:
RCV000992364
dbSNP Id:
rs41524046
COSMIC:
COSM1138362
COSM1138363
MyVariant Identifiers:
chrMT:g.3915G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.3915G>A , J01415.2:m.3915G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid change
ENST00000361390.2:c.609G>A
ENSP00000354687.2:p.Gly203=
Search 100 bp 5'
Search 100 bp 3'