ClinGen Allele Registry
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Canonical Allele Identifier:
CA88947467
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.176312308G>A
GRCh37
chr3:g.176030096G>A
Linked Data - Sequence & Population
gnomAD v3:
3:176312308 G / A
gnomAD v4:
chr3-176312308-G-A
Joint Max Group AF
0.00001919 (AFR)
Genomes Max Group AF
0.00001919 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6799767
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.176312308G>A , CM000665.2:g.176312308G>A
GRCh38
NC_000003.11:g.176030096G>A , CM000665.1:g.176030096G>A
GRCh37
NC_000003.10:g.177512790G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'