ClinGen Allele Registry
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Canonical Allele Identifier:
CA190687659
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.21408858A>C
GRCh37
chr9:g.21408857A>C
Linked Data - Sequence & Population
gnomAD v2:
9:21408857 A / C
gnomAD v3:
9:21408858 A / C
gnomAD v4:
chr9-21408858-A-C
Joint Max Group AF
0.21987562 (EAS)
Genomes Max Group AF
0.21987562 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12553612
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.21408858A>C , CM000671.2:g.21408858A>C
GRCh38
NC_000009.11:g.21408857A>C , CM000671.1:g.21408857A>C
GRCh37
NC_000009.10:g.21398857A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'