ClinGen Allele Registry
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Canonical Allele Identifier:
CA12032089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.100655944C>T
GRCh37
chr5:g.99991648C>T
Linked Data - Sequence & Population
gnomAD v2:
5:99991648 C / T
gnomAD v3:
5:100655944 C / T
gnomAD v4:
chr5-100655944-C-T
Joint Max Group AF
0.20116031 (EAS)
Genomes Max Group AF
0.20116031 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4702982
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.100655944C>T , CM000667.2:g.100655944C>T
GRCh38
NC_000005.9:g.99991648C>T , CM000667.1:g.99991648C>T
GRCh37
NC_000005.8:g.100019547C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'