ClinGen Allele Registry
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Canonical Allele Identifier:
CA11747537
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.25099962G>C
GRCh37
chr4:g.25101584G>C
Linked Data - Sequence & Population
gnomAD v2:
4:25101584 G / C
gnomAD v3:
4:25099962 G / C
gnomAD v4:
chr4-25099962-G-C
Joint Max Group AF
0.19023206 (MID)
Genomes Max Group AF
0.1878446 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17408391
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.25099962G>C , CM000666.2:g.25099962G>C
GRCh38
NC_000004.11:g.25101584G>C , CM000666.1:g.25101584G>C
GRCh37
NC_000004.10:g.24710682G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'