ClinGen Allele Registry
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Canonical Allele Identifier:
CA198901286
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806780G>A
GRCh37
chr9:g.117569060G>A
Linked Data - Sequence & Population
gnomAD v2:
9:117569060 G / A
gnomAD v3:
9:114806780 G / A
gnomAD v4:
chr9-114806780-G-A
Joint Max Group AF
0.0001468 (NFE)
Genomes Max Group AF
0.0001468 (NFE)
Linked Data - NCBI & NCI
dbSNP:
143595948
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806780G>A , CM000671.2:g.114806780G>A
GRCh38
NC_000009.11:g.117569060G>A , CM000671.1:g.117569060G>A
GRCh37
NC_000009.10:g.116608881G>A
NCBI36
NG_011488.2:g.4349C>T
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