ClinGen Allele Registry
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Canonical Allele Identifier:
CA15396668
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.10109273T>C
GRCh37
chr5:g.10109385T>C
Linked Data - Sequence & Population
gnomAD v2:
5:10109385 T / C
gnomAD v3:
5:10109273 T / C
gnomAD v4:
chr5-10109273-T-C
Joint Max Group AF
0.66540974 (AFR)
Genomes Max Group AF
0.66540974 (AFR)
Linked Data - NCBI & NCI
dbSNP:
906071
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.10109273T>C , CM000667.2:g.10109273T>C
GRCh38
NC_000005.9:g.10109385T>C , CM000667.1:g.10109385T>C
GRCh37
NC_000005.8:g.10162385T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'