ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15356773
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.75407765A>G
GRCh37
chr4:g.76332975A>G
Linked Data - Sequence & Population
gnomAD v2:
4:76332975 A / G
gnomAD v3:
4:75407765 A / G
gnomAD v4:
chr4-75407765-A-G
Joint Max Group AF
0.25051472 (NFE)
Genomes Max Group AF
0.25050754 (NFE)
Exomes Max Group AF
0.10945252 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2903698
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.75407765A>G , CM000666.2:g.75407765A>G
GRCh38
NC_000004.11:g.76332975A>G , CM000666.1:g.76332975A>G
GRCh37
NC_000004.10:g.76551999A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'