ClinGen Allele Registry
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Canonical Allele Identifier:
CA882068207
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.38645807C>G
Linked Data - Sequence & Population
gnomAD v3:
19:38645807 C / G
gnomAD v4:
chr19-38645807-C-G
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1177246710
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.38645807C>G , CM000681.2:g.38645807C>G
GRCh38
NC_000019.9:g.39136447C>G , CM000681.1:g.39136447C>G
GRCh37
NC_000019.8:g.43828287C>G
NCBI36
NG_007082.2:g.3121C>G
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