ClinGen Allele Registry
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Canonical Allele Identifier:
CA11387166
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.172452314C>T
GRCh37
chr3:g.172170104C>T
Linked Data - Sequence & Population
gnomAD v2:
3:172170104 C / T
gnomAD v3:
3:172452314 C / T
gnomAD v4:
chr3-172452314-C-T
Joint Max Group AF
0.4531275 (AFR)
Genomes Max Group AF
0.4531275 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9819506
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.172452314C>T , CM000665.2:g.172452314C>T
GRCh38
NC_000003.11:g.172170104C>T , CM000665.1:g.172170104C>T
GRCh37
NC_000003.10:g.173652798C>T
NCBI36
NG_021159.1:g.1143G>A
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