ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11878858
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.130729712G>A
GRCh37
chr4:g.131650867G>A
Linked Data - Sequence & Population
gnomAD v2:
4:131650867 G / A
gnomAD v3:
4:130729712 G / A
gnomAD v4:
chr4-130729712-G-A
Joint Max Group AF
0.08840479 (EAS)
Genomes Max Group AF
0.08840479 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17051076
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.130729712G>A , CM000666.2:g.130729712G>A
GRCh38
NC_000004.11:g.131650867G>A , CM000666.1:g.131650867G>A
GRCh37
NC_000004.10:g.131870317G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'