ClinGen Allele Registry
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Canonical Allele Identifier:
CA15357883
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.155134181C>A
GRCh37
chr4:g.156055333C>A
Linked Data - Sequence & Population
gnomAD v2:
4:156055333 C / A
gnomAD v3:
4:155134181 C / A
gnomAD v4:
chr4-155134181-C-A
Joint Max Group AF
0.80463129 (EAS)
Genomes Max Group AF
0.80463129 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1902491
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.155134181C>A , CM000666.2:g.155134181C>A
GRCh38
NC_000004.11:g.156055333C>A , CM000666.1:g.156055333C>A
GRCh37
NC_000004.10:g.156274783C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'