ClinGen Allele Registry
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Canonical Allele Identifier:
CA561687860
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.104872175G>A
GRCh37
chr5:g.104207876G>A
Linked Data - Sequence & Population
gnomAD v2:
5:104207876 G / A
gnomAD v3:
5:104872175 G / A
gnomAD v4:
chr5-104872175-G-A
Joint Max Group AF
0.00015876 (EAS)
Genomes Max Group AF
0.00015876 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1349827972
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.104872175G>A , CM000667.2:g.104872175G>A
GRCh38
NC_000005.9:g.104207876G>A , CM000667.1:g.104207876G>A
GRCh37
NC_000005.8:g.104235775G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'