ClinGen Allele Registry
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Canonical Allele Identifier:
CA12481968
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.128238730G>A
GRCh37
chr7:g.127878783G>A
Linked Data - Sequence & Population
gnomAD v2:
7:127878783 G / A
gnomAD v3:
7:128238730 G / A
gnomAD v4:
chr7-128238730-G-A
Joint Max Group AF
0.72418456 (EAS)
Genomes Max Group AF
0.72418456 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7799039
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.128238730G>A , CM000669.2:g.128238730G>A
GRCh38
NC_000007.13:g.127878783G>A , CM000669.1:g.127878783G>A
GRCh37
NC_000007.12:g.127666019G>A
NCBI36
NG_007450.1:g.2453G>A
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