ClinGen Allele Registry
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Canonical Allele Identifier:
CA12168600
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.42288491C>T
GRCh37
chr5:g.42288593C>T
Linked Data - Sequence & Population
gnomAD v2:
5:42288593 C / T
gnomAD v3:
5:42288491 C / T
gnomAD v4:
chr5-42288491-C-T
Joint Max Group AF
0.10044658 (AFR)
Genomes Max Group AF
0.10044658 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11748684
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.42288491C>T , CM000667.2:g.42288491C>T
GRCh38
NC_000005.9:g.42288593C>T , CM000667.1:g.42288593C>T
GRCh37
NC_000005.8:g.42324350C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'