ClinGen Allele Registry
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Canonical Allele Identifier:
CA13036089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.107394019C>T
GRCh37
chr9:g.110156300C>T
Linked Data - Sequence & Population
gnomAD v2:
9:110156300 C / T
gnomAD v3:
9:107394019 C / T
gnomAD v4:
chr9-107394019-C-T
Joint Max Group AF
0.87804715 (EAS)
Genomes Max Group AF
0.87804715 (EAS)
Linked Data - NCBI & NCI
dbSNP:
817826
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.107394019C>T , CM000671.2:g.107394019C>T
GRCh38
NC_000009.11:g.110156300C>T , CM000671.1:g.110156300C>T
GRCh37
NC_000009.10:g.109196121C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'