ClinGen Allele Registry
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Canonical Allele Identifier:
CA15350472
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.93965880T>C
GRCh37
chr4:g.94887031T>C
Linked Data - Sequence & Population
gnomAD v2:
4:94887031 T / C
gnomAD v3:
4:93965880 T / C
gnomAD v4:
chr4-93965880-T-C
Joint Max Group AF
0.44223142 (NFE)
Genomes Max Group AF
0.44223142 (NFE)
Linked Data - NCBI & NCI
dbSNP:
13130787
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.93965880T>C , CM000666.2:g.93965880T>C
GRCh38
NC_000004.11:g.94887031T>C , CM000666.1:g.94887031T>C
GRCh37
NC_000004.10:g.95106054T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'