ClinGen Allele Registry
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Canonical Allele Identifier:
CA202078445
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.3959705C>G
GRCh37
chr10:g.4001897C>G
Linked Data - Sequence & Population
gnomAD v3:
10:3959705 C / G
gnomAD v4:
chr10-3959705-C-G
Linked Data - NCBI & NCI
dbSNP:
2031573
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.3959705C>G , CM000672.2:g.3959705C>G
GRCh38
NC_000010.10:g.4001897C>G , CM000672.1:g.4001897C>G
GRCh37
NC_000010.9:g.3991897C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'