ClinGen Allele Registry
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Canonical Allele Identifier:
CA14497747
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr17:g.47757912G>A
GRCh37
chr17:g.45835278G>A
Linked Data - Sequence & Population
gnomAD v2:
17:45835278 G / A
gnomAD v3:
17:47757912 G / A
gnomAD v4:
chr17-47757912-G-A
Joint Max Group AF
0.15728632 (NFE)
Genomes Max Group AF
0.15728632 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11651000
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.47757912G>A , CM000679.2:g.47757912G>A
GRCh38
NC_000017.10:g.45835278G>A , CM000679.1:g.45835278G>A
GRCh37
NC_000017.9:g.43190277G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'