ClinGen Allele Registry
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Canonical Allele Identifier:
CA14372123
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.12144227A>G
GRCh37
chr17:g.12047544A>G
Linked Data - Sequence & Population
gnomAD v2:
17:12047544 A / G
gnomAD v3:
17:12144227 A / G
gnomAD v4:
chr17-12144227-A-G
Joint Max Group AF
0.56709433 (EAS)
Genomes Max Group AF
0.56709433 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1870584
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.12144227A>G , CM000679.2:g.12144227A>G
GRCh38
NC_000017.10:g.12047544A>G , CM000679.1:g.12047544A>G
GRCh37
NC_000017.9:g.11988269A>G
NCBI36
NG_033952.1:g.128410A>G
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