ClinGen Allele Registry
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Canonical Allele Identifier:
CA13000125
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.125190369A>T
GRCh37
chr9:g.127952648A>T
Linked Data - Sequence & Population
gnomAD v2:
9:127952648 A / T
gnomAD v3:
9:125190369 A / T
gnomAD v4:
chr9-125190369-A-T
Joint Max Group AF
0.52000755 (EAS)
Genomes Max Group AF
0.52000755 (EAS)
Linked Data - NCBI & NCI
dbSNP:
458046
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.125190369A>T , CM000671.2:g.125190369A>T
GRCh38
NC_000009.11:g.127952648A>T , CM000671.1:g.127952648A>T
GRCh37
NC_000009.10:g.126992469A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'