ClinGen Allele Registry
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Canonical Allele Identifier:
CA15750424
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.28002147A>G
GRCh37
chr12:g.28155080A>G
Linked Data - Sequence & Population
gnomAD v2:
12:28155080 A / G
gnomAD v3:
12:28002147 A / G
gnomAD v4:
chr12-28002147-A-G
Joint Max Group AF
0.18071785 (EAS)
Genomes Max Group AF
0.18071785 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10771399
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.28002147A>G , CM000674.2:g.28002147A>G
GRCh38
NC_000012.11:g.28155080A>G , CM000674.1:g.28155080A>G
GRCh37
NC_000012.10:g.28046347A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'