ClinGen Allele Registry
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Canonical Allele Identifier:
CA11697037
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.108706869A>C
GRCh37
chr4:g.109628025A>C
Linked Data - Sequence & Population
gnomAD v2:
4:109628025 A / C
gnomAD v3:
4:108706869 A / C
gnomAD v4:
chr4-108706869-A-C
Joint Max Group AF
0.19157861 (AFR)
Genomes Max Group AF
0.19157861 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10029851
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.108706869A>C , CM000666.2:g.108706869A>C
GRCh38
NC_000004.11:g.109628025A>C , CM000666.1:g.109628025A>C
GRCh37
NC_000004.10:g.109847474A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'