ClinGen Allele Registry
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Canonical Allele Identifier:
CA135231671
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.15243787C>G
GRCh37
chr6:g.15244018C>G
Linked Data - Sequence & Population
gnomAD v2:
6:15244018 C / G
gnomAD v3:
6:15243787 C / G
gnomAD v4:
chr6-15243787-C-G
Joint Max Group AF
0.02370054 (NFE)
Genomes Max Group AF
0.02370124 (NFE)
Linked Data - NCBI & NCI
dbSNP:
34229995
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.15243787C>G , CM000668.2:g.15243787C>G
GRCh38
NC_000006.11:g.15244018C>G , CM000668.1:g.15244018C>G
GRCh37
NC_000006.10:g.15351997C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'