ClinGen Allele Registry
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Canonical Allele Identifier:
CA11361731
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.55279372A>C
GRCh37
chr3:g.55313400A>C
Linked Data - Sequence & Population
gnomAD v2:
3:55313400 A / C
gnomAD v3:
3:55279372 A / C
gnomAD v4:
chr3-55279372-A-C
Joint Max Group AF
0.88956606 (SAS)
Genomes Max Group AF
0.88956606 (SAS)
Linked Data - NCBI & NCI
dbSNP:
358806
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.55279372A>C , CM000665.2:g.55279372A>C
GRCh38
NC_000003.11:g.55313400A>C , CM000665.1:g.55313400A>C
GRCh37
NC_000003.10:g.55288440A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'