ClinGen Allele Registry
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Canonical Allele Identifier:
CA308127703
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.38645811C>T
GRCh37
chr19:g.39136451C>T
Linked Data - Sequence & Population
gnomAD v3:
19:38645811 C / T
gnomAD v4:
chr19-38645811-C-T
Joint Max Group AF
0.00007873 (AFR)
Genomes Max Group AF
0.00007873 (AFR)
Linked Data - NCBI & NCI
dbSNP:
921144017
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.38645811C>T , CM000681.2:g.38645811C>T
GRCh38
NC_000019.9:g.39136451C>T , CM000681.1:g.39136451C>T
GRCh37
NC_000019.8:g.43828291C>T
NCBI36
NG_007082.2:g.3125C>T
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