ClinGen Allele Registry
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Canonical Allele Identifier:
CA13722145
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.28003148C>G
GRCh37
chr12:g.28156081C>G
Linked Data - Sequence & Population
gnomAD v2:
12:28156081 C / G
gnomAD v3:
12:28003148 C / G
gnomAD v4:
chr12-28003148-C-G
Joint Max Group AF
0.18058684 (EAS)
Genomes Max Group AF
0.18058684 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12371778
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.28003148C>G , CM000674.2:g.28003148C>G
GRCh38
NC_000012.11:g.28156081C>G , CM000674.1:g.28156081C>G
GRCh37
NC_000012.10:g.28047348C>G
NCBI36
Search 100 bp 5'
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