ClinGen Allele Registry
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Canonical Allele Identifier:
CA14380852
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr17:g.51153130A>T
GRCh37
chr17:g.49230491A>T
Linked Data - Sequence & Population
gnomAD v2:
17:49230491 A / T
gnomAD v3:
17:51153130 A / T
gnomAD v4:
chr17-51153130-A-T
Joint Max Group AF
0.39797136 (AMR)
Genomes Max Group AF
0.39797136 (AMR)
Linked Data - NCBI & NCI
dbSNP:
3760468
2151350551
2151350553
2151350556
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.51153130A>T , CM000679.2:g.51153130A>T
GRCh38
NC_000017.10:g.49230491A>T , CM000679.1:g.49230491A>T
GRCh37
NC_000017.9:g.46585490A>T
NCBI36
NG_021169.1:g.4572A>T
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