ClinGen Allele Registry
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Canonical Allele Identifier:
CA13757819
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.130922632A>G
GRCh37
chr12:g.131407177A>G
Linked Data - Sequence & Population
gnomAD v2:
12:131407177 A / G
gnomAD v3:
12:130922632 A / G
gnomAD v4:
chr12-130922632-A-G
Joint Max Group AF
0.90178351 (SAS)
Genomes Max Group AF
0.90178351 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4759802
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.130922632A>G , CM000674.2:g.130922632A>G
GRCh38
NC_000012.11:g.131407177A>G , CM000674.1:g.131407177A>G
GRCh37
NC_000012.10:g.129973130A>G
NCBI36
Search 100 bp 5'
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