ClinGen Allele Registry
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Canonical Allele Identifier:
CA590283342
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806779C>T
GRCh37
chr9:g.117569059C>T
Linked Data - Sequence & Population
gnomAD v2:
9:117569059 C / T
gnomAD v3:
9:114806779 C / T
gnomAD v4:
chr9-114806779-C-T
Linked Data - NCBI & NCI
dbSNP:
1405969102
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806779C>T , CM000671.2:g.114806779C>T
GRCh38
NC_000009.11:g.117569059C>T , CM000671.1:g.117569059C>T
GRCh37
NC_000009.10:g.116608880C>T
NCBI36
NG_011488.2:g.4350G>A
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