ClinGen Allele Registry
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Canonical Allele Identifier:
CA13632780
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.111369695G>A
GRCh37
chr12:g.111807499G>A
Linked Data - Sequence & Population
gnomAD v2:
12:111807499 G / A
gnomAD v3:
12:111369695 G / A
gnomAD v4:
chr12-111369695-G-A
Joint Max Group AF
0.90841214 (EAS)
Genomes Max Group AF
0.90841214 (EAS)
Linked Data - NCBI & NCI
dbSNP:
933399
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.111369695G>A , CM000674.2:g.111369695G>A
GRCh38
NC_000012.11:g.111807499G>A , CM000674.1:g.111807499G>A
GRCh37
NC_000012.10:g.110291882G>A
NCBI36
NG_021347.1:g.4427C>T
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