ClinGen Allele Registry
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Canonical Allele Identifier:
CA80573820
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.112657461T>C
GRCh37
chr3:g.112376308T>C
Linked Data - Sequence & Population
gnomAD v2:
3:112376308 T / C
gnomAD v3:
3:112657461 T / C
gnomAD v4:
chr3-112657461-T-C
Joint Max Group AF
0.29439857 (EAS)
Genomes Max Group AF
0.29439857 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12634229
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.112657461T>C , CM000665.2:g.112657461T>C
GRCh38
NC_000003.11:g.112376308T>C , CM000665.1:g.112376308T>C
GRCh37
NC_000003.10:g.113858998T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'