ClinGen Allele Registry
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Canonical Allele Identifier:
CA12977491
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.841152C>A
GRCh37
chr9:g.841152C>A
Linked Data - Sequence & Population
gnomAD v2:
9:841152 C / A
gnomAD v3:
9:841152 C / A
gnomAD v4:
chr9-841152-C-A
Joint Max Group AF
0.93130096 (NFE)
Genomes Max Group AF
0.93130096 (NFE)
Linked Data - NCBI & NCI
dbSNP:
912062
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.841152C>A , CM000671.2:g.841152C>A
GRCh38
NC_000009.11:g.841152C>A , CM000671.1:g.841152C>A
GRCh37
NC_000009.10:g.831152C>A
NCBI36
NG_009221.1:g.4463C>A
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