ClinGen Allele Registry
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Canonical Allele Identifier:
CA166107904
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.127606849G>A
GRCh37
chr7:g.127246903G>A
Linked Data - Sequence & Population
gnomAD v2:
7:127246903 G / A
gnomAD v3:
7:127606849 G / A
gnomAD v4:
chr7-127606849-G-A
Joint Max Group AF
0.31130741 (SAS)
Genomes Max Group AF
0.31130741 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10229583
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.127606849G>A , CM000669.2:g.127606849G>A
GRCh38
NC_000007.13:g.127246903G>A , CM000669.1:g.127246903G>A
GRCh37
NC_000007.12:g.127034139G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'