ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11650131
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.72779634G>A
GRCh37
chr4:g.73645351G>A
Linked Data - Sequence & Population
gnomAD v2:
4:73645351 G / A
gnomAD v3:
4:72779634 G / A
gnomAD v4:
chr4-72779634-G-A
Joint Max Group AF
0.25854277 (EAS)
Genomes Max Group AF
0.25854277 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12507628
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.72779634G>A , CM000666.2:g.72779634G>A
GRCh38
NC_000004.11:g.73645351G>A , CM000666.1:g.73645351G>A
GRCh37
NC_000004.10:g.73864215G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'