ClinGen Allele Registry
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Canonical Allele Identifier:
CA15249171
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.72343990G>C
GRCh37
chr3:g.72393141G>C
Linked Data - Sequence & Population
gnomAD v2:
3:72393141 G / C
gnomAD v3:
3:72343990 G / C
gnomAD v4:
chr3-72343990-G-C
Joint Max Group AF
0.71958805 (AFR)
Genomes Max Group AF
0.71958805 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9832740
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.72343990G>C , CM000665.2:g.72343990G>C
GRCh38
NC_000003.11:g.72393141G>C , CM000665.1:g.72393141G>C
GRCh37
NC_000003.10:g.72475831G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'