ClinGen Allele Registry
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Canonical Allele Identifier:
CA601114582
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.92965261C>A
GRCh37
chr11:g.92698427C>A
Linked Data - Sequence & Population
gnomAD v2:
11:92698427 C / A
gnomAD v3:
11:92965261 C / A
gnomAD v4:
chr11-92965261-C-A
Joint Max Group AF
0.00000801 (AFR)
Genomes Max Group AF
0.00000801 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10830962
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.92965261C>A , CM000673.2:g.92965261C>A
GRCh38
NC_000011.9:g.92698427C>A , CM000673.1:g.92698427C>A
GRCh37
NC_000011.8:g.92338075C>A
NCBI36
NG_028160.1:g.639C>A
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