ClinGen Allele Registry
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Canonical Allele Identifier:
CA13464263
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.73766000C>T
GRCh37
chr11:g.73477045C>T
Linked Data - Sequence & Population
gnomAD v2:
11:73477045 C / T
gnomAD v3:
11:73766000 C / T
gnomAD v4:
chr11-73766000-C-T
Joint Max Group AF
0.16046906 (AFR)
Genomes Max Group AF
0.16046906 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1723838
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.73766000C>T , CM000673.2:g.73766000C>T
GRCh38
NC_000011.9:g.73477045C>T , CM000673.1:g.73477045C>T
GRCh37
NC_000011.8:g.73154693C>T
NCBI36
NG_029821.1:g.157G>A
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