ClinGen Allele Registry
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Canonical Allele Identifier:
CA11747721
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.26061368A>G
GRCh37
chr4:g.26062990A>G
Linked Data - Sequence & Population
gnomAD v2:
4:26062990 A / G
gnomAD v3:
4:26061368 A / G
gnomAD v4:
chr4-26061368-A-G
Joint Max Group AF
0.21446014 (AFR)
Genomes Max Group AF
0.21446014 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10019888
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.26061368A>G , CM000666.2:g.26061368A>G
GRCh38
NC_000004.11:g.26062990A>G , CM000666.1:g.26062990A>G
GRCh37
NC_000004.10:g.25672088A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'