ClinGen Allele Registry
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Canonical Allele Identifier:
CA12733291
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.96493302T>C
GRCh37
chr8:g.97505530T>C
Linked Data - Sequence & Population
gnomAD v2:
8:97505530 T / C
gnomAD v3:
8:96493302 T / C
gnomAD v4:
chr8-96493302-T-C
Joint Max Group AF
0.34304605 (EAS)
Genomes Max Group AF
0.34304605 (EAS)
Linked Data - NCBI & NCI
dbSNP:
61599409
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.96493302T>C , CM000670.2:g.96493302T>C
GRCh38
NC_000008.10:g.97505530T>C , CM000670.1:g.97505530T>C
GRCh37
NC_000008.9:g.97574706T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'