ClinGen Allele Registry
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Canonical Allele Identifier:
CA12101871
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.87103445G>C
GRCh37
chr5:g.86399262G>C
Linked Data - Sequence & Population
gnomAD v2:
5:86399262 G / C
gnomAD v3:
5:87103445 G / C
gnomAD v4:
chr5-87103445-G-C
Joint Max Group AF
0.97517742 (EAS)
Genomes Max Group AF
0.97517742 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2544677
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.87103445G>C , CM000667.2:g.87103445G>C
GRCh38
NC_000005.9:g.86399262G>C , CM000667.1:g.86399262G>C
GRCh37
NC_000005.8:g.86435018G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'