ClinGen Allele Registry
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Canonical Allele Identifier:
CA14732187
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.47898636G>A
GRCh37
chr19:g.48401893G>A
Linked Data - Sequence & Population
gnomAD v2:
19:48401893 G / A
gnomAD v3:
19:47898636 G / A
gnomAD v4:
chr19-47898636-G-A
Joint Max Group AF
0.1539965 (NFE)
Genomes Max Group AF
0.1539965 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2637125
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.47898636G>A , CM000681.2:g.47898636G>A
GRCh38
NC_000019.9:g.48401893G>A , CM000681.1:g.48401893G>A
GRCh37
NC_000019.8:g.53093705G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'