ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11699796
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122825464A>C
GRCh37
chr4:g.123746619A>C
Linked Data - Sequence & Population
gnomAD v2:
4:123746619 A / C
gnomAD v3:
4:122825464 A / C
gnomAD v4:
chr4-122825464-A-C
Joint Max Group AF
0.60836047 (AFR)
Genomes Max Group AF
0.60836047 (AFR)
Linked Data - NCBI & NCI
dbSNP:
308393
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122825464A>C , CM000666.2:g.122825464A>C
GRCh38
NC_000004.11:g.123746619A>C , CM000666.1:g.123746619A>C
GRCh37
NC_000004.10:g.123966069A>C
NCBI36
NG_029067.1:g.3757A>C
NG_029067.2:g.3757A>C
Search 100 bp 5'
Search 100 bp 3'