ClinGen Allele Registry
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Canonical Allele Identifier:
CA228623312
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113407984T>G
GRCh37
chr11:g.113278706T>G
Linked Data - Sequence & Population
gnomAD v3:
11:113407984 T / G
gnomAD v4:
chr11-113407984-T-G
Joint Max Group AF
0.00003762 (NFE)
Genomes Max Group AF
0.00003762 (NFE)
Linked Data - NCBI & NCI
dbSNP:
930538324
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113407984T>G , CM000673.2:g.113407984T>G
GRCh38
NC_000011.9:g.113278706T>G , CM000673.1:g.113278706T>G
GRCh37
NC_000011.8:g.112783916T>G
NCBI36
NG_008841.1:g.72296A>C
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