ClinGen Allele Registry
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Canonical Allele Identifier:
CA15320136
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.10124321C>G
GRCh37
chr4:g.10125945C>G
Linked Data - Sequence & Population
gnomAD v2:
4:10125945 C / G
gnomAD v3:
4:10124321 C / G
gnomAD v4:
chr4-10124321-C-G
Joint Max Group AF
0.36622339 (EAS)
Genomes Max Group AF
0.36622339 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10516202
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.10124321C>G , CM000666.2:g.10124321C>G
GRCh38
NC_000004.11:g.10125945C>G , CM000666.1:g.10125945C>G
GRCh37
NC_000004.10:g.9735043C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'