ClinGen Allele Registry
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Canonical Allele Identifier:
CA12063693
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.132397705G>C
GRCh37
chr5:g.131733397G>C
Linked Data - Sequence & Population
gnomAD v2:
5:131733397 G / C
gnomAD v3:
5:132397705 G / C
gnomAD v4:
chr5-132397705-G-C
Joint Max Group AF
0.39449852 (NFE)
Genomes Max Group AF
0.39449852 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11739135
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.132397705G>C , CM000667.2:g.132397705G>C
GRCh38
NC_000005.9:g.131733397G>C , CM000667.1:g.131733397G>C
GRCh37
NC_000005.8:g.131761296G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'