ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11699797
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122825787C>G
GRCh37
chr4:g.123746942C>G
Linked Data - Sequence & Population
gnomAD v2:
4:123746942 C / G
gnomAD v3:
4:122825787 C / G
gnomAD v4:
chr4-122825787-C-G
Joint Max Group AF
0.64692004 (AFR)
Genomes Max Group AF
0.64692004 (AFR)
Linked Data - NCBI & NCI
dbSNP:
308395
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122825787C>G , CM000666.2:g.122825787C>G
GRCh38
NC_000004.11:g.123746942C>G , CM000666.1:g.123746942C>G
GRCh37
NC_000004.10:g.123966392C>G
NCBI36
NG_029067.1:g.4080C>G
NG_029067.2:g.4080C>G
Search 100 bp 5'
Search 100 bp 3'