ClinGen Allele Registry
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Canonical Allele Identifier:
CA14445845
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.14657699T>C
GRCh37
chr17:g.14561016T>C
Linked Data - Sequence & Population
gnomAD v2:
17:14561016 T / C
gnomAD v3:
17:14657699 T / C
gnomAD v4:
chr17-14657699-T-C
Joint Max Group AF
0.78992361 (AFR)
Genomes Max Group AF
0.78992361 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12940030
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.14657699T>C , CM000679.2:g.14657699T>C
GRCh38
NC_000017.10:g.14561016T>C , CM000679.1:g.14561016T>C
GRCh37
NC_000017.9:g.14501741T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'